Canonical Allele Identifier: CA389347649

Gene: COCH

Linked Data

• gnomAD v4: 14-30885484-A-T
• MyVariant Identifiers: chr14:g.31354690A>T (hg19) ; chr14:g.30885484A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885484A>T , CM000676.2:g.30885484A>T	GRCh38
NC_000014.8:g.31354690A>T , CM000676.1:g.31354690A>T	GRCh37
NC_000014.7:g.30424441A>T	NCBI36
NG_008211.2:g.15950A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1019A>T	ENSP00000216361.5:p.Asp340Val
ENST00000396618.9:c.824A>T MANE Select	ENSP00000379862.3:p.Asp275Val
ENST00000555117.2:c.881A>T	ENSP00000493569.1:p.Asp294Val
ENST00000643575.1:c.824A>T	ENSP00000494838.1:p.Asp275Val
ENST00000643697.1:n.1126A>T
ENST00000644874.2:c.824A>T	ENSP00000496360.1:p.Asp275Val
ENST00000216361.8:c.824A>T	ENSP00000216361.4:p.Asp275Val
ENST00000396618.7:c.824A>T	ENSP00000379862.3:p.Asp275Val
ENST00000460581.6:c.488A>T	ENSP00000451713.1:p.Asp163Val
ENST00000468826.2:c.475A>T
ENST00000475087.5:c.824A>T	ENSP00000451528.1:p.Asp275Val
ENST00000555881.5:c.470A>T	ENSP00000452569.1:p.Asp157Val
ENST00000557065.1:c.606A>T	ENSP00000451629.1:n.606A>T
NM_001135058.1:c.824A>T	NP_001128530.1:p.Asp275Val
NM_004086.2:c.824A>T	NP_004077.1:p.Asp275Val
NR_038356.1:n.1381T>A
XM_011536539.1:c.824A>T	XP_011534841.1:p.Asp275Val
NM_001347720.1:c.1019A>T	NP_001334649.1:p.Asp340Val
XM_017021071.1:c.1019A>T	XP_016876560.1:p.Asp340Val
XM_024449506.1:c.881A>T	XP_024305274.1:p.Asp294Val
NM_004086.3:c.824A>T MANE Select	NP_004077.1:p.Asp275Val
NM_001135058.2:c.824A>T	NP_001128530.1:p.Asp275Val
NM_001347720.2:c.1019A>T	NP_001334649.1:p.Asp340Val