Canonical Allele Identifier: CA2126951081

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30879207_30879208delinsAG , CM000676.2:g.30879207_30879208delinsAG	GRCh38
NC_000014.8:g.31348413_31348414delinsAG , CM000676.1:g.31348413_31348414delinsAG	GRCh37
NC_000014.7:g.30418164_30418165delinsAG	NCBI36
NG_008211.2:g.9673_9674delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.569-216_569-215delinsAG	ENSP00000216361.5:n.569-216_569-215delinsAG
ENST00000396618.9:c.374-216_374-215delinsAG MANE Select	ENSP00000379862.3:n.374-216_374-215delinsAG
ENST00000555117.2:c.374-216_374-215delinsAG	ENSP00000493569.1:n.374-216_374-215delinsAG
ENST00000643575.1:c.374-216_374-215delinsAG	ENSP00000494838.1:n.374-216_374-215delinsAG
ENST00000643697.1:n.619-216_619-215delinsAG
ENST00000644874.2:c.374-216_374-215delinsAG	ENSP00000496360.1:n.374-216_374-215delinsAG
ENST00000216361.8:c.374-216_374-215delinsAG	ENSP00000216361.4:n.374-216_374-215delinsAG
ENST00000396618.7:c.374-216_374-215delinsAG	ENSP00000379862.3:n.374-216_374-215delinsAG
ENST00000460581.6:c.38-216_38-215delinsAG	ENSP00000451713.1:n.38-216_38-215delinsAG
ENST00000475087.5:c.374-216_374-215delinsAG	ENSP00000451528.1:n.374-216_374-215delinsAG
ENST00000553772.5:c.240-1245_240-1244delinsAG	ENSP00000452343.1:n.240-1245_240-1244delinsAG
ENST00000553833.5:n.528-216_528-215delinsAG
ENST00000555881.5:c.83-1245_83-1244delinsAG	ENSP00000452569.1:n.83-1245_83-1244delinsAG
ENST00000556908.5:c.326-216_326-215delinsAG	ENSP00000452541.1:n.326-216_326-215delinsAG
ENST00000557065.1:c.156-216_156-215delinsAG	ENSP00000451629.1:n.156-216_156-215delinsAG
NM_001135058.1:c.374-216_374-215delinsAG	NP_001128530.1:n.374-216_374-215delinsAG
NM_004086.2:c.374-216_374-215delinsAG	NP_004077.1:n.374-216_374-215delinsAG
NR_038356.1:n.1618-2656_1618-2655delinsCT
XM_011536539.1:c.374-216_374-215delinsAG	XP_011534841.1:n.374-216_374-215delinsAG
NM_001347720.1:c.569-216_569-215delinsAG	NP_001334649.1:n.569-216_569-215delinsAG
XM_017021071.1:c.569-216_569-215delinsAG	XP_016876560.1:n.569-216_569-215delinsAG
XM_024449506.1:c.374-216_374-215delinsAG	XP_024305274.1:n.374-216_374-215delinsAG
NM_004086.3:c.374-216_374-215delinsAG MANE Select	NP_004077.1:n.374-216_374-215delinsAG
NM_001135058.2:c.374-216_374-215delinsAG	NP_001128530.1:n.374-216_374-215delinsAG
NM_001347720.2:c.569-216_569-215delinsAG	NP_001334649.1:n.569-216_569-215delinsAG