Canonical Allele Identifier: CA2126958148
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30885861C= , CM000676.2:g.30885861C= GRCh38
NC_000014.8:g.31355067C= , CM000676.1:g.31355067C= GRCh37
NC_000014.7:g.30424818C= NCBI36
NG_008211.2:g.16327C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216361.9:c.1221C= ENSP00000216361.5:p.Tyr407=
ENST00000396618.9:c.1026C= MANE Select ENSP00000379862.3:p.Tyr342=
ENST00000555117.2:c.1083C= ENSP00000493569.1:p.Tyr361=
ENST00000643575.1:c.1026C= ENSP00000494838.1:p.Tyr342=
ENST00000643697.1:n.1328C=
ENST00000644874.2:c.1026C= ENSP00000496360.1:p.Tyr342=
ENST00000216361.8:c.1026C= ENSP00000216361.4:p.Tyr342=
ENST00000396618.7:c.1026C= ENSP00000379862.3:p.Tyr342=
ENST00000460581.6:c.690C= ENSP00000451713.1:p.Tyr230=
ENST00000468826.2:c.677C=
ENST00000475087.5:c.1026C= ENSP00000451528.1:p.Tyr342=
NM_001135058.1:c.1026C= NP_001128530.1:p.Tyr342=
NM_004086.2:c.1026C= NP_004077.1:p.Tyr342=
NR_038356.1:n.1004G=
XM_011536539.1:c.1026C= XP_011534841.1:p.Tyr342=
NM_001347720.1:c.1221C= NP_001334649.1:p.Tyr407=
XM_017021071.1:c.1221C= XP_016876560.1:p.Tyr407=
XM_024449506.1:c.1083C= XP_024305274.1:p.Tyr361=
NM_004086.3:c.1026C= MANE Select NP_004077.1:p.Tyr342=
NM_001135058.2:c.1026C= NP_001128530.1:p.Tyr342=
NM_001347720.2:c.1221C= NP_001334649.1:p.Tyr407=