Canonical Allele Identifier: CA486083535

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31354916A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885710A>T , CM000676.2:g.30885710A>T	GRCh38
NC_000014.8:g.31354916A>T , CM000676.1:g.31354916A>T	GRCh37
NC_000014.7:g.30424667A>T	NCBI36
NG_008211.2:g.16176A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1156-86A>T	ENSP00000216361.5:n.1156-86A>T
ENST00000396618.9:c.961-86A>T MANE Select	ENSP00000379862.3:n.961-86A>T
ENST00000555117.2:c.1018-86A>T	ENSP00000493569.1:n.1018-86A>T
ENST00000643575.1:c.961-86A>T	ENSP00000494838.1:n.961-86A>T
ENST00000643697.1:n.1263-86A>T
ENST00000644874.2:c.961-86A>T	ENSP00000496360.1:n.961-86A>T
ENST00000216361.8:c.961-86A>T	ENSP00000216361.4:n.961-86A>T
ENST00000396618.7:c.961-86A>T	ENSP00000379862.3:n.961-86A>T
ENST00000460581.6:c.625-86A>T	ENSP00000451713.1:n.625-86A>T
ENST00000468826.2:c.612-86A>T
ENST00000475087.5:c.961-86A>T	ENSP00000451528.1:n.961-86A>T
NM_001135058.1:c.961-86A>T	NP_001128530.1:n.961-86A>T
NM_004086.2:c.961-86A>T	NP_004077.1:n.961-86A>T
NR_038356.1:n.1155T>A
XM_011536539.1:c.961-86A>T	XP_011534841.1:n.961-86A>T
NM_001347720.1:c.1156-86A>T	NP_001334649.1:n.1156-86A>T
XM_017021071.1:c.1156-86A>T	XP_016876560.1:n.1156-86A>T
XM_024449506.1:c.1018-86A>T	XP_024305274.1:n.1018-86A>T
NM_004086.3:c.961-86A>T MANE Select	NP_004077.1:n.961-86A>T
NM_001135058.2:c.961-86A>T	NP_001128530.1:n.961-86A>T
NM_001347720.2:c.1156-86A>T	NP_001334649.1:n.1156-86A>T