Canonical Allele Identifier: CA1140629941

Gene: ERMAP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42830851G= , CM000663.2:g.42830851G=	GRCh38
NC_000001.10:g.43296522G= , CM000663.1:g.43296522G=	GRCh37
NC_000001.9:g.43069109G=	NCBI36
NG_008749.1:g.18747G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.169G= MANE Select	ENSP00000361595.2:p.Gly57=
ENST00000487556.6:n.452-4187G=
ENST00000642150.1:n.356G=
ENST00000647120.1:n.248-4187G=
ENST00000328249.3:c.-102G=	ENSP00000332439.3:n.-102G=
ENST00000372514.7:c.169G=	ENSP00000361592.3:p.Gly57=
ENST00000372517.6:c.169G=	ENSP00000361595.2:p.Gly57=
ENST00000487556.5:n.247-4187G=
NM_001017922.1:c.169G=	NP_001017922.1:p.Gly57=
NM_018538.3:c.169G=	NP_061008.2:p.Gly57=
XM_006710313.2:c.169G=	XP_006710376.1:p.Gly57=
XM_011540570.1:c.169G=	XP_011538872.1:p.Gly57=
XM_011540571.1:c.169G=	XP_011538873.1:p.Gly57=
XM_006710313.4:c.169G=	XP_006710376.1:p.Gly57=
XM_011540570.3:c.169G=	XP_011538872.1:p.Gly57=
XM_011540571.3:c.169G=	XP_011538873.1:p.Gly57=
NM_001017922.2:c.169G= MANE Select	NP_001017922.1:p.Gly57=
NM_018538.4:c.169G=	NP_061008.2:p.Gly57=