Canonical Allele Identifier: CA417542845

Gene: ERMAP

Linked Data

• MyVariant Identifiers: chr1:g.43296560A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42830889A>T , CM000663.2:g.42830889A>T	GRCh38
NC_000001.10:g.43296560A>T , CM000663.1:g.43296560A>T	GRCh37
NC_000001.9:g.43069147A>T	NCBI36
NG_008749.1:g.18785A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.207A>T MANE Select	ENSP00000361595.2:p.Pro69=
ENST00000487556.6:n.452-4149A>T
ENST00000642150.1:n.394A>T
ENST00000647120.1:n.248-4149A>T
ENST00000328249.3:c.-64A>T	ENSP00000332439.3:n.-64A>T
ENST00000372514.7:c.207A>T	ENSP00000361592.3:p.Pro69=
ENST00000372517.6:c.207A>T	ENSP00000361595.2:p.Pro69=
ENST00000487556.5:n.247-4149A>T
NM_001017922.1:c.207A>T	NP_001017922.1:p.Pro69=
NM_018538.3:c.207A>T	NP_061008.2:p.Pro69=
XM_006710313.2:c.207A>T	XP_006710376.1:p.Pro69=
XM_011540570.1:c.207A>T	XP_011538872.1:p.Pro69=
XM_011540571.1:c.207A>T	XP_011538873.1:p.Pro69=
XM_006710313.4:c.207A>T	XP_006710376.1:p.Pro69=
XM_011540570.3:c.207A>T	XP_011538872.1:p.Pro69=
XM_011540571.3:c.207A>T	XP_011538873.1:p.Pro69=
NM_001017922.2:c.207A>T MANE Select	NP_001017922.1:p.Pro69=
NM_018538.4:c.207A>T	NP_061008.2:p.Pro69=