Canonical Allele Identifier: CA1165371686

Gene: ERMAP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831008T= , CM000663.2:g.42831008T=	GRCh38
NC_000001.10:g.43296679T= , CM000663.1:g.43296679T=	GRCh37
NC_000001.9:g.43069266T=	NCBI36
NG_008749.1:g.18904T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.326T= MANE Select	ENSP00000361595.2:p.Val109=
ENST00000487556.6:n.452-4030T=
ENST00000642150.1:n.513T=
ENST00000647120.1:n.248-4030T=
ENST00000328249.3:c.56T=	ENSP00000332439.3:p.Val19=
ENST00000372514.7:c.326T=	ENSP00000361592.3:p.Val109=
ENST00000372517.6:c.326T=	ENSP00000361595.2:p.Val109=
ENST00000487556.5:n.247-4030T=
NM_001017922.1:c.326T=	NP_001017922.1:p.Val109=
NM_018538.3:c.326T=	NP_061008.2:p.Val109=
XM_006710313.2:c.326T=	XP_006710376.1:p.Val109=
XM_011540570.1:c.326T=	XP_011538872.1:p.Val109=
XM_011540571.1:c.326T=	XP_011538873.1:p.Val109=
XM_006710313.4:c.326T=	XP_006710376.1:p.Val109=
XM_011540570.3:c.326T=	XP_011538872.1:p.Val109=
XM_011540571.3:c.326T=	XP_011538873.1:p.Val109=
NM_001017922.2:c.326T= MANE Select	NP_001017922.1:p.Val109=
NM_018538.4:c.326T=	NP_061008.2:p.Val109=