Canonical Allele Identifier: CA2126950430

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30878654_30878658delinsCAAAT , CM000676.2:g.30878654_30878658delinsCAAAT	GRCh38
NC_000014.8:g.31347860_31347864delinsCAAAT , CM000676.1:g.31347860_31347864delinsCAAAT	GRCh37
NC_000014.7:g.30417611_30417615delinsCAAAT	NCBI36
NG_008211.2:g.9120_9124delinsCAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.435-157_435-153delinsCAAAT	ENSP00000216361.5:n.435-157_435-153delinsCAAAT
ENST00000396618.9:c.240-157_240-153delinsCAAAT MANE Select	ENSP00000379862.3:n.240-157_240-153delinsCAAAT
ENST00000555117.2:c.240-157_240-153delinsCAAAT	ENSP00000493569.1:n.240-157_240-153delinsCAAAT
ENST00000643575.1:c.240-157_240-153delinsCAAAT	ENSP00000494838.1:n.240-157_240-153delinsCAAAT
ENST00000643697.1:n.485-157_485-153delinsCAAAT
ENST00000644874.2:c.240-157_240-153delinsCAAAT	ENSP00000496360.1:n.240-157_240-153delinsCAAAT
ENST00000216361.8:c.240-157_240-153delinsCAAAT	ENSP00000216361.4:n.240-157_240-153delinsCAAAT
ENST00000396618.7:c.240-157_240-153delinsCAAAT	ENSP00000379862.3:n.240-157_240-153delinsCAAAT
ENST00000460581.6:c.-97-157_-97-153delinsCAAAT	ENSP00000451713.1:n.-97-157_-97-153delinsCAAAT
ENST00000475087.5:c.240-157_240-153delinsCAAAT	ENSP00000451528.1:n.240-157_240-153delinsCAAAT
ENST00000553772.5:c.239+926_239+930delinsCAAAT	ENSP00000452343.1:n.239+926_239+930delinsCAAAT
ENST00000553833.5:n.394-157_394-153delinsCAAAT
ENST00000555881.5:c.83-1798_83-1794delinsCAAAT	ENSP00000452569.1:n.83-1798_83-1794delinsCAAAT
ENST00000556908.5:c.192-157_192-153delinsCAAAT	ENSP00000452541.1:n.192-157_192-153delinsCAAAT
ENST00000557065.1:c.156-769_156-765delinsCAAAT	ENSP00000451629.1:n.156-769_156-765delinsCAAAT
NM_001135058.1:c.240-157_240-153delinsCAAAT	NP_001128530.1:n.240-157_240-153delinsCAAAT
NM_004086.2:c.240-157_240-153delinsCAAAT	NP_004077.1:n.240-157_240-153delinsCAAAT
NR_038356.1:n.1618-2106_1618-2102delinsATTTG
XM_011536539.1:c.240-157_240-153delinsCAAAT	XP_011534841.1:n.240-157_240-153delinsCAAAT
NM_001347720.1:c.435-157_435-153delinsCAAAT	NP_001334649.1:n.435-157_435-153delinsCAAAT
XM_017021071.1:c.435-157_435-153delinsCAAAT	XP_016876560.1:n.435-157_435-153delinsCAAAT
XM_024449506.1:c.240-157_240-153delinsCAAAT	XP_024305274.1:n.240-157_240-153delinsCAAAT
NM_004086.3:c.240-157_240-153delinsCAAAT MANE Select	NP_004077.1:n.240-157_240-153delinsCAAAT
NM_001135058.2:c.240-157_240-153delinsCAAAT	NP_001128530.1:n.240-157_240-153delinsCAAAT
NM_001347720.2:c.435-157_435-153delinsCAAAT	NP_001334649.1:n.435-157_435-153delinsCAAAT