Canonical Allele Identifier: CA1165371722

Gene: ERMAP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831097G= , CM000663.2:g.42831097G=	GRCh38
NC_000001.10:g.43296768G= , CM000663.1:g.43296768G=	GRCh37
NC_000001.9:g.43069355G=	NCBI36
NG_008749.1:g.18993G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.415G= MANE Select	ENSP00000361595.2:p.Val139=
ENST00000487556.6:n.452-3941G=
ENST00000642150.1:n.602G=
ENST00000647120.1:n.248-3941G=
ENST00000328249.3:c.145G=	ENSP00000332439.3:p.Val49=
ENST00000372514.7:c.415G=	ENSP00000361592.3:p.Val139=
ENST00000372517.6:c.415G=	ENSP00000361595.2:p.Val139=
ENST00000487556.5:n.247-3941G=
NM_001017922.1:c.415G=	NP_001017922.1:p.Val139=
NM_018538.3:c.415G=	NP_061008.2:p.Val139=
XM_006710313.2:c.415G=	XP_006710376.1:p.Val139=
XM_011540570.1:c.415G=	XP_011538872.1:p.Val139=
XM_011540571.1:c.415G=	XP_011538873.1:p.Val139=
XM_006710313.4:c.415G=	XP_006710376.1:p.Val139=
XM_011540570.3:c.415G=	XP_011538872.1:p.Val139=
XM_011540571.3:c.415G=	XP_011538873.1:p.Val139=
NM_001017922.2:c.415G= MANE Select	NP_001017922.1:p.Val139=
NM_018538.4:c.415G=	NP_061008.2:p.Val139=