Canonical Allele Identifier: CA2126960752
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30889676C= , CM000676.2:g.30889676C= GRCh38
NC_000014.8:g.31358882C= , CM000676.1:g.31358882C= GRCh37
NC_000014.7:g.30428633C= NCBI36
NG_008211.2:g.20142C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216361.9:c.1733C= ENSP00000216361.5:p.Ala578=
ENST00000396618.9:c.1538C= MANE Select ENSP00000379862.3:p.Ala513=
ENST00000555117.2:c.1534+3364C= ENSP00000493569.1:n.1534+3364C=
ENST00000643575.1:c.1538C= ENSP00000494838.1:p.Ala513=
ENST00000643697.1:n.1840C=
ENST00000644874.2:c.1538C= ENSP00000496360.1:p.Ala513=
ENST00000216361.8:c.1538C= ENSP00000216361.4:p.Ala513=
ENST00000396618.7:c.1538C= ENSP00000379862.3:p.Ala513=
ENST00000460581.6:c.1202C= ENSP00000451713.1:p.Ala401=
ENST00000468826.2:c.1189C=
ENST00000475087.5:c.1477+3364C= ENSP00000451528.1:n.1477+3364C=
NM_001135058.1:c.1538C= NP_001128530.1:p.Ala513=
NM_004086.2:c.1538C= NP_004077.1:p.Ala513=
NR_038356.1:n.133G=
XM_011536539.1:c.1538C= XP_011534841.1:p.Ala513=
NM_001347720.1:c.1733C= NP_001334649.1:p.Ala578=
XM_017021071.1:c.1733C= XP_016876560.1:p.Ala578=
XM_024449506.1:c.1595C= XP_024305274.1:p.Ala532=
NM_004086.3:c.1538C= MANE Select NP_004077.1:p.Ala513=
NM_001135058.2:c.1538C= NP_001128530.1:p.Ala513=
NM_001347720.2:c.1733C= NP_001334649.1:p.Ala578=