Canonical Allele Identifier: CA389347706

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31354714A>T (hg19) ; chr14:g.30885508A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885508A>T , CM000676.2:g.30885508A>T	GRCh38
NC_000014.8:g.31354714A>T , CM000676.1:g.31354714A>T	GRCh37
NC_000014.7:g.30424465A>T	NCBI36
NG_008211.2:g.15974A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1043A>T	ENSP00000216361.5:p.Glu348Val
ENST00000396618.9:c.848A>T MANE Select	ENSP00000379862.3:p.Glu283Val
ENST00000555117.2:c.905A>T	ENSP00000493569.1:p.Glu302Val
ENST00000643575.1:c.848A>T	ENSP00000494838.1:p.Glu283Val
ENST00000643697.1:n.1150A>T
ENST00000644874.2:c.848A>T	ENSP00000496360.1:p.Glu283Val
ENST00000216361.8:c.848A>T	ENSP00000216361.4:p.Glu283Val
ENST00000396618.7:c.848A>T	ENSP00000379862.3:p.Glu283Val
ENST00000460581.6:c.512A>T	ENSP00000451713.1:p.Glu171Val
ENST00000468826.2:c.499A>T
ENST00000475087.5:c.848A>T	ENSP00000451528.1:p.Glu283Val
ENST00000555881.5:c.494A>T	ENSP00000452569.1:p.Glu165Val
ENST00000557065.1:c.630A>T	ENSP00000451629.1:n.630A>T
NM_001135058.1:c.848A>T	NP_001128530.1:p.Glu283Val
NM_004086.2:c.848A>T	NP_004077.1:p.Glu283Val
NR_038356.1:n.1357T>A
XM_011536539.1:c.848A>T	XP_011534841.1:p.Glu283Val
NM_001347720.1:c.1043A>T	NP_001334649.1:p.Glu348Val
XM_017021071.1:c.1043A>T	XP_016876560.1:p.Glu348Val
XM_024449506.1:c.905A>T	XP_024305274.1:p.Glu302Val
NM_004086.3:c.848A>T MANE Select	NP_004077.1:p.Glu283Val
NM_001135058.2:c.848A>T	NP_001128530.1:p.Glu283Val
NM_001347720.2:c.1043A>T	NP_001334649.1:p.Glu348Val