Canonical Allele Identifier: CA2126961323

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30890232_30890234delinsTAC , CM000676.2:g.30890232_30890234delinsTAC	GRCh38
NC_000014.8:g.31359438_31359440delinsTAC , CM000676.1:g.31359438_31359440delinsTAC	GRCh37
NC_000014.7:g.30429189_30429191delinsTAC	NCBI36
NG_008211.2:g.20698_20700delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396618.9:c.*441_*443delinsTAC MANE Select	ENSP00000379862.3:n.*441_*443delinsTAC
ENST00000555117.2:c.1534+3920_1534+3922delinsTAC	ENSP00000493569.1:n.1534+3920_1534+3922delinsTAC
ENST00000643575.1:c.*2+439_*2+441delinsTAC	ENSP00000494838.1:n.*2+439_*2+441delinsTAC
ENST00000644874.2:c.*441_*443delinsTAC	ENSP00000496360.1:n.*441_*443delinsTAC
ENST00000396618.7:c.*441_*443delinsTAC	ENSP00000379862.3:n.*441_*443delinsTAC
ENST00000460581.6:c.*441_*443delinsTAC	ENSP00000451713.1:n.*441_*443delinsTAC
ENST00000468826.2:c.1745_1747delinsTAC
ENST00000475087.5:c.1477+3920_1477+3922delinsTAC	ENSP00000451528.1:n.1477+3920_1477+3922delinsTAC
NM_001135058.1:c.*441_*443delinsTAC	NP_001128530.1:n.*441_*443delinsTAC
NM_004086.2:c.*441_*443delinsTAC	NP_004077.1:n.*441_*443delinsTAC
XM_011536539.1:c.*2+439_*2+441delinsTAC	XP_011534841.1:n.*2+439_*2+441delinsTAC
NM_001347720.1:c.*441_*443delinsTAC	NP_001334649.1:n.*441_*443delinsTAC
XM_017021071.1:c.*441_*443delinsTAC	XP_016876560.1:n.*441_*443delinsTAC
XM_024449506.1:c.*441_*443delinsTAC	XP_024305274.1:n.*441_*443delinsTAC
NM_004086.3:c.*441_*443delinsTAC MANE Select	NP_004077.1:n.*441_*443delinsTAC
NM_001135058.2:c.*441_*443delinsTAC	NP_001128530.1:n.*441_*443delinsTAC
NM_001347720.2:c.*441_*443delinsTAC	NP_001334649.1:n.*441_*443delinsTAC