Canonical Allele Identifier: CA2126957495
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30885501G= , CM000676.2:g.30885501G= GRCh38
NC_000014.8:g.31354707G= , CM000676.1:g.31354707G= GRCh37
NC_000014.7:g.30424458G= NCBI36
NG_008211.2:g.15967G=

Transcript Alleles

HGVS Amino-acid change
ENST00000216361.9:c.1036G= ENSP00000216361.5:p.Asp346=
ENST00000396618.9:c.841G= MANE Select ENSP00000379862.3:p.Asp281=
ENST00000555117.2:c.898G= ENSP00000493569.1:p.Asp300=
ENST00000643575.1:c.841G= ENSP00000494838.1:p.Asp281=
ENST00000643697.1:n.1143G=
ENST00000644874.2:c.841G= ENSP00000496360.1:p.Asp281=
ENST00000216361.8:c.841G= ENSP00000216361.4:p.Asp281=
ENST00000396618.7:c.841G= ENSP00000379862.3:p.Asp281=
ENST00000460581.6:c.505G= ENSP00000451713.1:p.Asp169=
ENST00000468826.2:c.492G=
ENST00000475087.5:c.841G= ENSP00000451528.1:p.Asp281=
ENST00000555881.5:c.487G= ENSP00000452569.1:p.Asp163=
ENST00000557065.1:c.623G= ENSP00000451629.1:n.623G=
NM_001135058.1:c.841G= NP_001128530.1:p.Asp281=
NM_004086.2:c.841G= NP_004077.1:p.Asp281=
NR_038356.1:n.1364C=
XM_011536539.1:c.841G= XP_011534841.1:p.Asp281=
NM_001347720.1:c.1036G= NP_001334649.1:p.Asp346=
XM_017021071.1:c.1036G= XP_016876560.1:p.Asp346=
XM_024449506.1:c.898G= XP_024305274.1:p.Asp300=
NM_004086.3:c.841G= MANE Select NP_004077.1:p.Asp281=
NM_001135058.2:c.841G= NP_001128530.1:p.Asp281=
NM_001347720.2:c.1036G= NP_001334649.1:p.Asp346=