Canonical Allele Identifier: CA389349675

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31358937A>T (hg19) ; chr14:g.30889731A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30889731A>T , CM000676.2:g.30889731A>T	GRCh38
NC_000014.8:g.31358937A>T , CM000676.1:g.31358937A>T	GRCh37
NC_000014.7:g.30428688A>T	NCBI36
NG_008211.2:g.20197A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1788A>T	ENSP00000216361.5:p.Glu596Asp
ENST00000396618.9:c.1593A>T MANE Select	ENSP00000379862.3:p.Glu531Asp
ENST00000555117.2:c.1534+3419A>T	ENSP00000493569.1:n.1534+3419A>T
ENST00000643575.1:c.1593A>T	ENSP00000494838.1:p.Glu531Asp
ENST00000643697.1:n.1895A>T
ENST00000644874.2:c.1593A>T	ENSP00000496360.1:p.Glu531Asp
ENST00000216361.8:c.1593A>T	ENSP00000216361.4:p.Glu531Asp
ENST00000396618.7:c.1593A>T	ENSP00000379862.3:p.Glu531Asp
ENST00000460581.6:c.1257A>T	ENSP00000451713.1:p.Glu419Asp
ENST00000468826.2:c.1244A>T
ENST00000475087.5:c.1477+3419A>T	ENSP00000451528.1:n.1477+3419A>T
NM_001135058.1:c.1593A>T	NP_001128530.1:p.Glu531Asp
NM_004086.2:c.1593A>T	NP_004077.1:p.Glu531Asp
NR_038356.1:n.78T>A
XM_011536539.1:c.1593A>T	XP_011534841.1:p.Glu531Asp
NM_001347720.1:c.1788A>T	NP_001334649.1:p.Glu596Asp
XM_017021071.1:c.1788A>T	XP_016876560.1:p.Glu596Asp
XM_024449506.1:c.1650A>T	XP_024305274.1:p.Glu550Asp
NM_004086.3:c.1593A>T MANE Select	NP_004077.1:p.Glu531Asp
NM_001135058.2:c.1593A>T	NP_001128530.1:p.Glu531Asp
NM_001347720.2:c.1788A>T	NP_001334649.1:p.Glu596Asp