Canonical Allele Identifier: CA389347379

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31354614C>G (hg19) ; chr14:g.30885408C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30885408C>G , CM000676.2:g.30885408C>G	GRCh38
NC_000014.8:g.31354614C>G , CM000676.1:g.31354614C>G	GRCh37
NC_000014.7:g.30424365C>G	NCBI36
NG_008211.2:g.15874C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000216361.9:c.943C>G	ENSP00000216361.5:p.His315Asp
ENST00000396618.9:c.748C>G MANE Select	ENSP00000379862.3:p.His250Asp
ENST00000555117.2:c.805C>G	ENSP00000493569.1:p.His269Asp
ENST00000643575.1:c.748C>G	ENSP00000494838.1:p.His250Asp
ENST00000643697.1:n.1050C>G
ENST00000644874.2:c.748C>G	ENSP00000496360.1:p.His250Asp
ENST00000216361.8:c.748C>G	ENSP00000216361.4:p.His250Asp
ENST00000396618.7:c.748C>G	ENSP00000379862.3:p.His250Asp
ENST00000460581.6:c.412C>G	ENSP00000451713.1:p.His138Asp
ENST00000468826.2:c.399C>G
ENST00000475087.5:c.748C>G	ENSP00000451528.1:p.His250Asp
ENST00000555881.5:c.394C>G	ENSP00000452569.1:p.His132Asp
ENST00000557065.1:c.530C>G	ENSP00000451629.1:n.530C>G
NM_001135058.1:c.748C>G	NP_001128530.1:p.His250Asp
NM_004086.2:c.748C>G	NP_004077.1:p.His250Asp
NR_038356.1:n.1452+5G>C
XM_011536539.1:c.748C>G	XP_011534841.1:p.His250Asp
NM_001347720.1:c.943C>G	NP_001334649.1:p.His315Asp
XM_017021071.1:c.943C>G	XP_016876560.1:p.His315Asp
XM_024449506.1:c.805C>G	XP_024305274.1:p.His269Asp
NM_004086.3:c.748C>G MANE Select	NP_004077.1:p.His250Asp
NM_001135058.2:c.748C>G	NP_001128530.1:p.His250Asp
NM_001347720.2:c.943C>G	NP_001334649.1:p.His315Asp