Canonical Allele Identifier: CA389347670

Gene: COCH

Linked Data

• COSMIC: COSM3955979 ; COSM3955980
• MyVariant Identifiers: chr14:g.31354699C>A (hg19) ; chr14:g.30885493C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885493C>A , CM000676.2:g.30885493C>A	GRCh38
NC_000014.8:g.31354699C>A , CM000676.1:g.31354699C>A	GRCh37
NC_000014.7:g.30424450C>A	NCBI36
NG_008211.2:g.15959C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1028C>A	ENSP00000216361.5:p.Pro343His
ENST00000396618.9:c.833C>A MANE Select	ENSP00000379862.3:p.Pro278His
ENST00000555117.2:c.890C>A	ENSP00000493569.1:p.Pro297His
ENST00000643575.1:c.833C>A	ENSP00000494838.1:p.Pro278His
ENST00000643697.1:n.1135C>A
ENST00000644874.2:c.833C>A	ENSP00000496360.1:p.Pro278His
ENST00000216361.8:c.833C>A	ENSP00000216361.4:p.Pro278His
ENST00000396618.7:c.833C>A	ENSP00000379862.3:p.Pro278His
ENST00000460581.6:c.497C>A	ENSP00000451713.1:p.Pro166His
ENST00000468826.2:c.484C>A
ENST00000475087.5:c.833C>A	ENSP00000451528.1:p.Pro278His
ENST00000555881.5:c.479C>A	ENSP00000452569.1:p.Pro160His
ENST00000557065.1:c.615C>A	ENSP00000451629.1:n.615C>A
NM_001135058.1:c.833C>A	NP_001128530.1:p.Pro278His
NM_004086.2:c.833C>A	NP_004077.1:p.Pro278His
NR_038356.1:n.1372G>T
XM_011536539.1:c.833C>A	XP_011534841.1:p.Pro278His
NM_001347720.1:c.1028C>A	NP_001334649.1:p.Pro343His
XM_017021071.1:c.1028C>A	XP_016876560.1:p.Pro343His
XM_024449506.1:c.890C>A	XP_024305274.1:p.Pro297His
NM_004086.3:c.833C>A MANE Select	NP_004077.1:p.Pro278His
NM_001135058.2:c.833C>A	NP_001128530.1:p.Pro278His
NM_001347720.2:c.1028C>A	NP_001334649.1:p.Pro343His