Canonical Allele Identifier: CA485832227

Gene: COCH

Linked Data

• dbSNP Id: rs1473899659
• gnomAD v4: 14-30885434-A-T
• MyVariant Identifiers: chr14:g.31354640A>T (hg19) ; chr14:g.30885434A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885434A>T , CM000676.2:g.30885434A>T	GRCh38
NC_000014.8:g.31354640A>T , CM000676.1:g.31354640A>T	GRCh37
NC_000014.7:g.30424391A>T	NCBI36
NG_008211.2:g.15900A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.969A>T	ENSP00000216361.5:p.Val323=
ENST00000396618.9:c.774A>T MANE Select	ENSP00000379862.3:p.Val258=
ENST00000555117.2:c.831A>T	ENSP00000493569.1:p.Val277=
ENST00000643575.1:c.774A>T	ENSP00000494838.1:p.Val258=
ENST00000643697.1:n.1076A>T
ENST00000644874.2:c.774A>T	ENSP00000496360.1:p.Val258=
ENST00000216361.8:c.774A>T	ENSP00000216361.4:p.Val258=
ENST00000396618.7:c.774A>T	ENSP00000379862.3:p.Val258=
ENST00000460581.6:c.438A>T	ENSP00000451713.1:p.Val146=
ENST00000468826.2:c.425A>T
ENST00000475087.5:c.774A>T	ENSP00000451528.1:p.Val258=
ENST00000555881.5:c.420A>T	ENSP00000452569.1:p.Val140=
ENST00000557065.1:c.556A>T	ENSP00000451629.1:n.556A>T
NM_001135058.1:c.774A>T	NP_001128530.1:p.Val258=
NM_004086.2:c.774A>T	NP_004077.1:p.Val258=
NR_038356.1:n.1431T>A
XM_011536539.1:c.774A>T	XP_011534841.1:p.Val258=
NM_001347720.1:c.969A>T	NP_001334649.1:p.Val323=
XM_017021071.1:c.969A>T	XP_016876560.1:p.Val323=
XM_024449506.1:c.831A>T	XP_024305274.1:p.Val277=
NM_004086.3:c.774A>T MANE Select	NP_004077.1:p.Val258=
NM_001135058.2:c.774A>T	NP_001128530.1:p.Val258=
NM_001347720.2:c.969A>T	NP_001334649.1:p.Val323=