Canonical Allele Identifier: CA2126950574

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30878800_30878802delinsTTG , CM000676.2:g.30878800_30878802delinsTTG	GRCh38
NC_000014.8:g.31348006_31348008delinsTTG , CM000676.1:g.31348006_31348008delinsTTG	GRCh37
NC_000014.7:g.30417757_30417759delinsTTG	NCBI36
NG_008211.2:g.9266_9268delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.435-11_435-9delinsTTG	ENSP00000216361.5:n.435-11_435-9delinsTTG
ENST00000396618.9:c.240-11_240-9delinsTTG MANE Select	ENSP00000379862.3:n.240-11_240-9delinsTTG
ENST00000555117.2:c.240-11_240-9delinsTTG	ENSP00000493569.1:n.240-11_240-9delinsTTG
ENST00000643575.1:c.240-11_240-9delinsTTG	ENSP00000494838.1:n.240-11_240-9delinsTTG
ENST00000643697.1:n.485-11_485-9delinsTTG
ENST00000644874.2:c.240-11_240-9delinsTTG	ENSP00000496360.1:n.240-11_240-9delinsTTG
ENST00000216361.8:c.240-11_240-9delinsTTG	ENSP00000216361.4:n.240-11_240-9delinsTTG
ENST00000396618.7:c.240-11_240-9delinsTTG	ENSP00000379862.3:n.240-11_240-9delinsTTG
ENST00000460581.6:c.-97-11_-97-9delinsTTG	ENSP00000451713.1:n.-97-11_-97-9delinsTTG
ENST00000475087.5:c.240-11_240-9delinsTTG	ENSP00000451528.1:n.240-11_240-9delinsTTG
ENST00000553772.5:c.239+1072_239+1074delinsTTG	ENSP00000452343.1:n.239+1072_239+1074delinsTTG
ENST00000553833.5:n.394-11_394-9delinsTTG
ENST00000555881.5:c.83-1652_83-1650delinsTTG	ENSP00000452569.1:n.83-1652_83-1650delinsTTG
ENST00000556908.5:c.192-11_192-9delinsTTG	ENSP00000452541.1:n.192-11_192-9delinsTTG
ENST00000557065.1:c.156-623_156-621delinsTTG	ENSP00000451629.1:n.156-623_156-621delinsTTG
NM_001135058.1:c.240-11_240-9delinsTTG	NP_001128530.1:n.240-11_240-9delinsTTG
NM_004086.2:c.240-11_240-9delinsTTG	NP_004077.1:n.240-11_240-9delinsTTG
NR_038356.1:n.1618-2250_1618-2248delinsCAA
XM_011536539.1:c.240-11_240-9delinsTTG	XP_011534841.1:n.240-11_240-9delinsTTG
NM_001347720.1:c.435-11_435-9delinsTTG	NP_001334649.1:n.435-11_435-9delinsTTG
XM_017021071.1:c.435-11_435-9delinsTTG	XP_016876560.1:n.435-11_435-9delinsTTG
XM_024449506.1:c.240-11_240-9delinsTTG	XP_024305274.1:n.240-11_240-9delinsTTG
NM_004086.3:c.240-11_240-9delinsTTG MANE Select	NP_004077.1:n.240-11_240-9delinsTTG
NM_001135058.2:c.240-11_240-9delinsTTG	NP_001128530.1:n.240-11_240-9delinsTTG
NM_001347720.2:c.435-11_435-9delinsTTG	NP_001334649.1:n.435-11_435-9delinsTTG