Canonical Allele Identifier: CA1143453626

Gene: ERMAP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42830895G= , CM000663.2:g.42830895G=	GRCh38
NC_000001.10:g.43296566G= , CM000663.1:g.43296566G=	GRCh37
NC_000001.9:g.43069153G=	NCBI36
NG_008749.1:g.18791G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.213G= MANE Select	ENSP00000361595.2:p.Pro71=
ENST00000487556.6:n.452-4143G=
ENST00000642150.1:n.400G=
ENST00000647120.1:n.248-4143G=
ENST00000328249.3:c.-58G=	ENSP00000332439.3:n.-58G=
ENST00000372514.7:c.213G=	ENSP00000361592.3:p.Pro71=
ENST00000372517.6:c.213G=	ENSP00000361595.2:p.Pro71=
ENST00000487556.5:n.247-4143G=
NM_001017922.1:c.213G=	NP_001017922.1:p.Pro71=
NM_018538.3:c.213G=	NP_061008.2:p.Pro71=
XM_006710313.2:c.213G=	XP_006710376.1:p.Pro71=
XM_011540570.1:c.213G=	XP_011538872.1:p.Pro71=
XM_011540571.1:c.213G=	XP_011538873.1:p.Pro71=
XM_006710313.4:c.213G=	XP_006710376.1:p.Pro71=
XM_011540570.3:c.213G=	XP_011538872.1:p.Pro71=
XM_011540571.3:c.213G=	XP_011538873.1:p.Pro71=
NM_001017922.2:c.213G= MANE Select	NP_001017922.1:p.Pro71=
NM_018538.4:c.213G=	NP_061008.2:p.Pro71=