Canonical Allele Identifier: CA1165371687

Gene: ERMAP

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831010_42831012delinsACT , CM000663.2:g.42831010_42831012delinsACT	GRCh38
NC_000001.10:g.43296681_43296683delinsACT , CM000663.1:g.43296681_43296683delinsACT	GRCh37
NC_000001.9:g.43069268_43069270delinsACT	NCBI36
NG_008749.1:g.18906_18908delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.328_330delinsACT MANE Select	ENSP00000361595.2:p.Thr110=
ENST00000487556.6:n.452-4028_452-4026delinsACT
ENST00000642150.1:n.515_517delinsACT
ENST00000647120.1:n.248-4028_248-4026delinsACT
ENST00000328249.3:c.58_60delinsACT	ENSP00000332439.3:p.Thr20=
ENST00000372514.7:c.328_330delinsACT	ENSP00000361592.3:p.Thr110=
ENST00000372517.6:c.328_330delinsACT	ENSP00000361595.2:p.Thr110=
ENST00000487556.5:n.247-4028_247-4026delinsACT
NM_001017922.1:c.328_330delinsACT	NP_001017922.1:p.Thr110=
NM_018538.3:c.328_330delinsACT	NP_061008.2:p.Thr110=
XM_006710313.2:c.328_330delinsACT	XP_006710376.1:p.Thr110=
XM_011540570.1:c.328_330delinsACT	XP_011538872.1:p.Thr110=
XM_011540571.1:c.328_330delinsACT	XP_011538873.1:p.Thr110=
XM_006710313.4:c.328_330delinsACT	XP_006710376.1:p.Thr110=
XM_011540570.3:c.328_330delinsACT	XP_011538872.1:p.Thr110=
XM_011540571.3:c.328_330delinsACT	XP_011538873.1:p.Thr110=
NM_001017922.2:c.328_330delinsACT MANE Select	NP_001017922.1:p.Thr110=
NM_018538.4:c.328_330delinsACT	NP_061008.2:p.Thr110=