Canonical Allele Identifier: CA7142874

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30874929A>G , CM000676.2:g.30874929A>G	GRCh38
NC_000014.8:g.31344135A>G , CM000676.1:g.31344135A>G	GRCh37
NC_000014.7:g.30413886A>G	NCBI36
NG_008211.2:g.5395A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.-10A>G	ENSP00000216361.5:n.-10A>G
ENST00000396618.9:c.-10A>G MANE Select	ENSP00000379862.3:n.-10A>G
ENST00000555117.2:c.-10A>G	ENSP00000493569.1:n.-10A>G
ENST00000643575.1:c.-10A>G	ENSP00000494838.1:n.-10A>G
ENST00000644874.2:c.-10A>G	ENSP00000496360.1:n.-10A>G
ENST00000216361.8:c.-10A>G	ENSP00000216361.4:n.-10A>G
ENST00000396618.7:c.-10A>G	ENSP00000379862.3:n.-10A>G
ENST00000460581.6:c.-381A>G	ENSP00000451713.1:n.-381A>G
ENST00000475087.5:c.-10A>G	ENSP00000451528.1:n.-10A>G
ENST00000553772.5:c.-10A>G	ENSP00000452343.1:n.-10A>G
ENST00000555117.1:n.416A>G
ENST00000555881.5:c.-10A>G	ENSP00000452569.1:n.-10A>G
ENST00000556908.5:c.-10A>G	ENSP00000452541.1:n.-10A>G
NM_001135058.1:c.-10A>G	NP_001128530.1:n.-10A>G
NM_004086.2:c.-10A>G	NP_004077.1:n.-10A>G
XM_011536539.1:c.-10A>G	XP_011534841.1:n.-10A>G
NM_001347720.1:c.-10A>G	NP_001334649.1:n.-10A>G
XM_017021071.1:c.-10A>G	XP_016876560.1:n.-10A>G
XM_024449506.1:c.-10A>G	XP_024305274.1:n.-10A>G
NM_004086.3:c.-10A>G MANE Select	NP_004077.1:n.-10A>G
NM_001135058.2:c.-10A>G	NP_001128530.1:n.-10A>G
NM_001347720.2:c.-10A>G	NP_001334649.1:n.-10A>G