Canonical Allele Identifier: CA389347656

Gene: COCH

Linked Data

• gnomAD v4: 14-30885487-G-A
• MyVariant Identifiers: chr14:g.31354693G>A (hg19) ; chr14:g.30885487G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885487G>A , CM000676.2:g.30885487G>A	GRCh38
NC_000014.8:g.31354693G>A , CM000676.1:g.31354693G>A	GRCh37
NC_000014.7:g.30424444G>A	NCBI36
NG_008211.2:g.15953G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1022G>A	ENSP00000216361.5:p.Gly341Asp
ENST00000396618.9:c.827G>A MANE Select	ENSP00000379862.3:p.Gly276Asp
ENST00000555117.2:c.884G>A	ENSP00000493569.1:p.Gly295Asp
ENST00000643575.1:c.827G>A	ENSP00000494838.1:p.Gly276Asp
ENST00000643697.1:n.1129G>A
ENST00000644874.2:c.827G>A	ENSP00000496360.1:p.Gly276Asp
ENST00000216361.8:c.827G>A	ENSP00000216361.4:p.Gly276Asp
ENST00000396618.7:c.827G>A	ENSP00000379862.3:p.Gly276Asp
ENST00000460581.6:c.491G>A	ENSP00000451713.1:p.Gly164Asp
ENST00000468826.2:c.478G>A
ENST00000475087.5:c.827G>A	ENSP00000451528.1:p.Gly276Asp
ENST00000555881.5:c.473G>A	ENSP00000452569.1:p.Gly158Asp
ENST00000557065.1:c.609G>A	ENSP00000451629.1:n.609G>A
NM_001135058.1:c.827G>A	NP_001128530.1:p.Gly276Asp
NM_004086.2:c.827G>A	NP_004077.1:p.Gly276Asp
NR_038356.1:n.1378C>T
XM_011536539.1:c.827G>A	XP_011534841.1:p.Gly276Asp
NM_001347720.1:c.1022G>A	NP_001334649.1:p.Gly341Asp
XM_017021071.1:c.1022G>A	XP_016876560.1:p.Gly341Asp
XM_024449506.1:c.884G>A	XP_024305274.1:p.Gly295Asp
NM_004086.3:c.827G>A MANE Select	NP_004077.1:p.Gly276Asp
NM_001135058.2:c.827G>A	NP_001128530.1:p.Gly276Asp
NM_001347720.2:c.1022G>A	NP_001334649.1:p.Gly341Asp