Canonical Allele Identifier: CA486083957

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31355232T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30886026T>C , CM000676.2:g.30886026T>C	GRCh38
NC_000014.8:g.31355232T>C , CM000676.1:g.31355232T>C	GRCh37
NC_000014.7:g.30424983T>C	NCBI36
NG_008211.2:g.16492T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1386T>C	ENSP00000216361.5:p.Phe462=
ENST00000396618.9:c.1191T>C MANE Select	ENSP00000379862.3:p.Phe397=
ENST00000555117.2:c.1248T>C	ENSP00000493569.1:p.Phe416=
ENST00000643575.1:c.1191T>C	ENSP00000494838.1:p.Phe397=
ENST00000643697.1:n.1493T>C
ENST00000644874.2:c.1191T>C	ENSP00000496360.1:p.Phe397=
ENST00000216361.8:c.1191T>C	ENSP00000216361.4:p.Phe397=
ENST00000396618.7:c.1191T>C	ENSP00000379862.3:p.Phe397=
ENST00000460581.6:c.855T>C	ENSP00000451713.1:p.Phe285=
ENST00000468826.2:c.842T>C
ENST00000475087.5:c.1191T>C	ENSP00000451528.1:p.Phe397=
NM_001135058.1:c.1191T>C	NP_001128530.1:p.Phe397=
NM_004086.2:c.1191T>C	NP_004077.1:p.Phe397=
NR_038356.1:n.839A>G
XM_011536539.1:c.1191T>C	XP_011534841.1:p.Phe397=
NM_001347720.1:c.1386T>C	NP_001334649.1:p.Phe462=
XM_017021071.1:c.1386T>C	XP_016876560.1:p.Phe462=
XM_024449506.1:c.1248T>C	XP_024305274.1:p.Phe416=
NM_004086.3:c.1191T>C MANE Select	NP_004077.1:p.Phe397=
NM_001135058.2:c.1191T>C	NP_001128530.1:p.Phe397=
NM_001347720.2:c.1386T>C	NP_001334649.1:p.Phe462=