Canonical Allele Identifier: CA417543110

Gene: ERMAP

Linked Data

• MyVariant Identifiers: chr1:g.43296767C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831096C>G , CM000663.2:g.42831096C>G	GRCh38
NC_000001.10:g.43296767C>G , CM000663.1:g.43296767C>G	GRCh37
NC_000001.9:g.43069354C>G	NCBI36
NG_008749.1:g.18992C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.414C>G MANE Select	ENSP00000361595.2:p.Thr138=
ENST00000487556.6:n.452-3942C>G
ENST00000642150.1:n.601C>G
ENST00000647120.1:n.248-3942C>G
ENST00000328249.3:c.144C>G	ENSP00000332439.3:p.Thr48=
ENST00000372514.7:c.414C>G	ENSP00000361592.3:p.Thr138=
ENST00000372517.6:c.414C>G	ENSP00000361595.2:p.Thr138=
ENST00000487556.5:n.247-3942C>G
NM_001017922.1:c.414C>G	NP_001017922.1:p.Thr138=
NM_018538.3:c.414C>G	NP_061008.2:p.Thr138=
XM_006710313.2:c.414C>G	XP_006710376.1:p.Thr138=
XM_011540570.1:c.414C>G	XP_011538872.1:p.Thr138=
XM_011540571.1:c.414C>G	XP_011538873.1:p.Thr138=
XM_006710313.4:c.414C>G	XP_006710376.1:p.Thr138=
XM_011540570.3:c.414C>G	XP_011538872.1:p.Thr138=
XM_011540571.3:c.414C>G	XP_011538873.1:p.Thr138=
NM_001017922.2:c.414C>G MANE Select	NP_001017922.1:p.Thr138=
NM_018538.4:c.414C>G	NP_061008.2:p.Thr138=