Transcript #00005332 (NM_012307.2, EPB41L3 gene)

Transcript name erythrocyte membrane protein band 4.1-like 3
Gene name EPB41L3 (erythrocyte membrane protein band 4.1-like 3)
Chromosome 18
Transcript - NCBI ID NM_012307.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_036439.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

221 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-11-24C>A r.(=) p.(=)
?/? c.61G>A r.(?) p.(Glu21Lys)
?/? c.73G>A r.(?) p.(Ala25Thr)
?/? c.107C>A r.(?) p.(Pro36Gln)
?/? c.129G>A r.(=) p.(=)
?/? c.158C>T r.(?) p.(Ala53Val)
?/? c.176G>A r.(?) p.(Arg59Gln)
?/? c.184-31A>G r.(=) p.(=)
?/? c.184-3C>T r.spl? p.?
?/? c.262T>C r.(?) p.(Ser88Pro)
?/? c.273A>C r.(=) p.(=)
?/? c.293G>A r.(?) p.(Arg98Gln)
?/? c.326G>T r.(?) p.(Ser109Ile)
?/? c.351C>T r.(=) p.(=)
?/? c.381+12T>A r.(=) p.(=)
?/? c.382-4G>A r.spl? p.?
?/? c.385C>A r.(?) p.(Arg129Ser)
?/? c.467G>A r.(?) p.(Arg156Gln)
?/? c.487-69_487-68del r.(=) p.(=)
?/? c.487-13A>G r.(=) p.(=)
?/? c.529+24_529+25insT r.(=) p.(=)
?/? c.529+60del r.(=) p.(=)
?/? c.529+58_529+61del r.(=) p.(=)
?/? c.554A>G r.(?) p.(Asn185Ser)
?/? c.606-29C>T r.(=) p.(=)
?/? c.607T>G r.(?) p.(Tyr203Asp)
?/? c.625T>C r.(=) p.(=)
?/? c.690C>T r.(=) p.(=)
?/? c.696T>C r.(=) p.(=)
?/? c.708G>A r.(=) p.(=)
?/? c.717C>T r.(=) p.(=)
?/? c.760C>T r.(?) p.(Arg254Cys)
?/? c.768A>G r.(=) p.(=)
?/? c.824+9C>T r.(=) p.(=)
?/? c.824+49G>A r.(=) p.(=)
?/? c.825-19A>G r.(=) p.(=)
?/? c.825-15T>G r.(=) p.(=)
?/? c.851T>G r.(?) p.(Met284Arg)
?/? c.900A>G r.(=) p.(=)
?/? c.913-17T>G r.(=) p.(=)
?/? c.1055G>A r.(?) p.(Arg352Gln)
?/? c.1059G>A r.(=) p.(=)
?/? c.1065+27G>A r.(=) p.(=)
?/? c.1065+41T>G r.(=) p.(=)
?/? c.1065+42C>G r.(=) p.(=)
?/? c.1065+47A>G r.(=) p.(=)
?/? c.1066-28A>C r.(=) p.(=)
?/? c.1066-18G>C r.(=) p.(=)
?/? c.1066-9T>G r.(=) p.(=)
?/? c.1066-7_1066-6insT r.(=) p.(=)
?/? c.1067T>A r.(?) p.(Phe356Tyr)
?/? c.1074A>G r.(=) p.(=)
?/? c.1107C>T r.(=) p.(=)
?/? c.1149T>C r.(=) p.(=)
?/? c.1164-47A>G r.(=) p.(=)
?/? c.1164-11A>G r.(=) p.(=)
?/? c.1164-7T>A r.(=) p.(=)
?/? c.1212C>T r.(=) p.(=)
?/? c.1284T>G r.(=) p.(=)
?/? c.1339+10G>A r.(=) p.(=)
?/? c.1339+24A>G r.(=) p.(=)
?/? c.1339+35A>G r.(=) p.(=)
?/? c.1339+49del r.(=) p.(=)
?/? c.1365A>G r.(=) p.(=)
?/? c.1418A>G r.(?) p.(Lys473Arg)
?/? c.1462G>A r.(?) p.(Gly488Arg)
?/? c.1475C>A r.(?) p.(Thr492Lys)
?/? c.1493G>A r.(?) p.(Arg498Gln)
?/? c.1506+7C>G r.(=) p.(=)
?/? c.1507-22_1507-21del r.(=) p.(=)
?/? c.1553C>T r.(?) p.(Thr518Ile)
?/? c.1566C>T r.(=) p.(=)
?/? c.1585C>T r.(?) p.(Arg529Cys)
?/? c.1595G>A r.(?) p.(Cys532Tyr)
?/? c.1609T>C r.(?) p.(Cys537Arg)
?/? c.1621G>A r.(?) p.(Gly541Ser)
?/? c.1631C>T r.(?) p.(Pro544Leu)
?/? c.1663G>A r.(?) p.(Ala555Thr)
?/? c.1711G>C r.(?) p.(Val571Leu)
?/? c.1724A>G r.(?) p.(Tyr575Cys)
?/? c.1739G>A r.(?) p.(Gly580Asp)
?/? c.1772A>G r.(?) p.(Gln591Arg)
?/? c.1875C>T r.(=) p.(=)
?/? c.1877C>T r.(?) p.(Pro626Leu)
?/? c.1878G>A r.(=) p.(=)
?/? c.1882C>T r.(?) p.(Arg628Cys)
?/? c.1893C>T r.(=) p.(=)
?/? c.1956C>T r.(=) p.(=)
?/? c.1957G>A r.(?) p.(Ala653Thr)
?/? c.1964C>A r.(?) p.(Thr655Asn)
?/? c.1966C>T r.(?) p.(Leu656Phe)
?/? c.1981G>A r.(?) p.(Ala661Thr)
?/? c.2013G>A r.(=) p.(=)
?/? c.2026G>A r.(?) p.(Ala676Thr)
?/? c.2039A>G r.(?) p.(Asn680Ser)
?/? c.2067+9C>A r.(=) p.(=)
?/? c.2067+24G>A r.(=) p.(=)
?/? c.2067+35G>A r.(=) p.(=)
?/? c.2068-41del r.(=) p.(=)
?/? c.2068-6C>G r.(=) p.(=)
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