Canonical Allele Identifier: CA389347806

Gene: COCH

Linked Data

• dbSNP Id: rs1895757433
• gnomAD v4: 14-30885554-A-G
• MyVariant Identifiers: chr14:g.31354760A>G (hg19) ; chr14:g.30885554A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885554A>G , CM000676.2:g.30885554A>G	GRCh38
NC_000014.8:g.31354760A>G , CM000676.1:g.31354760A>G	GRCh37
NC_000014.7:g.30424511A>G	NCBI36
NG_008211.2:g.16020A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1089A>G	ENSP00000216361.5:p.Ile363Met
ENST00000396618.9:c.894A>G MANE Select	ENSP00000379862.3:p.Ile298Met
ENST00000555117.2:c.951A>G	ENSP00000493569.1:p.Ile317Met
ENST00000643575.1:c.894A>G	ENSP00000494838.1:p.Ile298Met
ENST00000643697.1:n.1196A>G
ENST00000644874.2:c.894A>G	ENSP00000496360.1:p.Ile298Met
ENST00000216361.8:c.894A>G	ENSP00000216361.4:p.Ile298Met
ENST00000396618.7:c.894A>G	ENSP00000379862.3:p.Ile298Met
ENST00000460581.6:c.558A>G	ENSP00000451713.1:p.Ile186Met
ENST00000468826.2:c.545A>G
ENST00000475087.5:c.894A>G	ENSP00000451528.1:p.Ile298Met
ENST00000555881.5:c.540A>G	ENSP00000452569.1:p.Ile180Met
NM_001135058.1:c.894A>G	NP_001128530.1:p.Ile298Met
NM_004086.2:c.894A>G	NP_004077.1:p.Ile298Met
NR_038356.1:n.1311T>C
XM_011536539.1:c.894A>G	XP_011534841.1:p.Ile298Met
NM_001347720.1:c.1089A>G	NP_001334649.1:p.Ile363Met
XM_017021071.1:c.1089A>G	XP_016876560.1:p.Ile363Met
XM_024449506.1:c.951A>G	XP_024305274.1:p.Ile317Met
NM_004086.3:c.894A>G MANE Select	NP_004077.1:p.Ile298Met
NM_001135058.2:c.894A>G	NP_001128530.1:p.Ile298Met
NM_001347720.2:c.1089A>G	NP_001334649.1:p.Ile363Met