Canonical Allele Identifier: CA389347416

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31354624A>T (hg19) ; chr14:g.30885418A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885418A>T , CM000676.2:g.30885418A>T	GRCh38
NC_000014.8:g.31354624A>T , CM000676.1:g.31354624A>T	GRCh37
NC_000014.7:g.30424375A>T	NCBI36
NG_008211.2:g.15884A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.953A>T	ENSP00000216361.5:p.Gln318Leu
ENST00000396618.9:c.758A>T MANE Select	ENSP00000379862.3:p.Gln253Leu
ENST00000555117.2:c.815A>T	ENSP00000493569.1:p.Gln272Leu
ENST00000643575.1:c.758A>T	ENSP00000494838.1:p.Gln253Leu
ENST00000643697.1:n.1060A>T
ENST00000644874.2:c.758A>T	ENSP00000496360.1:p.Gln253Leu
ENST00000216361.8:c.758A>T	ENSP00000216361.4:p.Gln253Leu
ENST00000396618.7:c.758A>T	ENSP00000379862.3:p.Gln253Leu
ENST00000460581.6:c.422A>T	ENSP00000451713.1:p.Gln141Leu
ENST00000468826.2:c.409A>T
ENST00000475087.5:c.758A>T	ENSP00000451528.1:p.Gln253Leu
ENST00000555881.5:c.404A>T	ENSP00000452569.1:p.Gln135Leu
ENST00000557065.1:c.540A>T	ENSP00000451629.1:n.540A>T
NM_001135058.1:c.758A>T	NP_001128530.1:p.Gln253Leu
NM_004086.2:c.758A>T	NP_004077.1:p.Gln253Leu
NR_038356.1:n.1447T>A
XM_011536539.1:c.758A>T	XP_011534841.1:p.Gln253Leu
NM_001347720.1:c.953A>T	NP_001334649.1:p.Gln318Leu
XM_017021071.1:c.953A>T	XP_016876560.1:p.Gln318Leu
XM_024449506.1:c.815A>T	XP_024305274.1:p.Gln272Leu
NM_004086.3:c.758A>T MANE Select	NP_004077.1:p.Gln253Leu
NM_001135058.2:c.758A>T	NP_001128530.1:p.Gln253Leu
NM_001347720.2:c.953A>T	NP_001334649.1:p.Gln318Leu