Canonical Allele Identifier: CA485832251

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31354667C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885461C>G , CM000676.2:g.30885461C>G	GRCh38
NC_000014.8:g.31354667C>G , CM000676.1:g.31354667C>G	GRCh37
NC_000014.7:g.30424418C>G	NCBI36
NG_008211.2:g.15927C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.996C>G	ENSP00000216361.5:p.Pro332=
ENST00000396618.9:c.801C>G MANE Select	ENSP00000379862.3:p.Pro267=
ENST00000555117.2:c.858C>G	ENSP00000493569.1:p.Pro286=
ENST00000643575.1:c.801C>G	ENSP00000494838.1:p.Pro267=
ENST00000643697.1:n.1103C>G
ENST00000644874.2:c.801C>G	ENSP00000496360.1:p.Pro267=
ENST00000216361.8:c.801C>G	ENSP00000216361.4:p.Pro267=
ENST00000396618.7:c.801C>G	ENSP00000379862.3:p.Pro267=
ENST00000460581.6:c.465C>G	ENSP00000451713.1:p.Pro155=
ENST00000468826.2:c.452C>G
ENST00000475087.5:c.801C>G	ENSP00000451528.1:p.Pro267=
ENST00000555881.5:c.447C>G	ENSP00000452569.1:p.Pro149=
ENST00000557065.1:c.583C>G	ENSP00000451629.1:n.583C>G
NM_001135058.1:c.801C>G	NP_001128530.1:p.Pro267=
NM_004086.2:c.801C>G	NP_004077.1:p.Pro267=
NR_038356.1:n.1404G>C
XM_011536539.1:c.801C>G	XP_011534841.1:p.Pro267=
NM_001347720.1:c.996C>G	NP_001334649.1:p.Pro332=
XM_017021071.1:c.996C>G	XP_016876560.1:p.Pro332=
XM_024449506.1:c.858C>G	XP_024305274.1:p.Pro286=
NM_004086.3:c.801C>G MANE Select	NP_004077.1:p.Pro267=
NM_001135058.2:c.801C>G	NP_001128530.1:p.Pro267=
NM_001347720.2:c.996C>G	NP_001334649.1:p.Pro332=