Canonical Allele Identifier: CA2126961029
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30889833C= , CM000676.2:g.30889833C= GRCh38
NC_000014.8:g.31359039C= , CM000676.1:g.31359039C= GRCh37
NC_000014.7:g.30428790C= NCBI36
NG_008211.2:g.20299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216361.9:c.*42C= ENSP00000216361.5:n.*42C=
ENST00000396618.9:c.*42C= MANE Select ENSP00000379862.3:n.*42C=
ENST00000555117.2:c.1534+3521C= ENSP00000493569.1:n.1534+3521C=
ENST00000643575.1:c.*2+40C= ENSP00000494838.1:n.*2+40C=
ENST00000643697.1:n.1997C=
ENST00000644874.2:c.*42C= ENSP00000496360.1:n.*42C=
ENST00000216361.8:c.*42C= ENSP00000216361.4:n.*42C=
ENST00000396618.7:c.*42C= ENSP00000379862.3:n.*42C=
ENST00000460581.6:c.*42C= ENSP00000451713.1:n.*42C=
ENST00000468826.2:c.1346C=
ENST00000475087.5:c.1477+3521C= ENSP00000451528.1:n.1477+3521C=
NM_001135058.1:c.*42C= NP_001128530.1:n.*42C=
NM_004086.2:c.*42C= NP_004077.1:n.*42C=
XM_011536539.1:c.*2+40C= XP_011534841.1:n.*2+40C=
NM_001347720.1:c.*42C= NP_001334649.1:n.*42C=
XM_017021071.1:c.*42C= XP_016876560.1:n.*42C=
XM_024449506.1:c.*42C= XP_024305274.1:n.*42C=
NM_004086.3:c.*42C= MANE Select NP_004077.1:n.*42C=
NM_001135058.2:c.*42C= NP_001128530.1:n.*42C=
NM_001347720.2:c.*42C= NP_001334649.1:n.*42C=