Canonical Allele Identifier: CA1190276598

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677927A= , CM000663.2:g.114677927A=	GRCh38
NC_000001.10:g.115220548A= , CM000663.1:g.115220548A=	GRCh37
NC_000001.9:g.115022071A=	NCBI36
NG_008012.1:g.22629T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1195T=	ENSP00000358551.4:p.Phe399=
ENST00000520113.7:c.1207T= MANE Select	ENSP00000430075.3:p.Phe403=
ENST00000637080.1:c.990T=	ENSP00000489753.1:n.990T=
ENST00000639077.1:n.872T=
ENST00000369538.3:c.1294T=	ENSP00000358551.3:p.Phe432=
ENST00000520113.6:c.1306T=	ENSP00000430075.2:p.Phe436=
NM_000036.2:c.1306T=	NP_000027.2:p.Phe436=
NM_001172626.1:c.1294T=	NP_001166097.1:p.Phe432=
NM_000036.3:c.1207T= MANE Select	NP_000027.3:p.Phe403=
NM_001172626.2:c.1195T=	NP_001166097.2:p.Phe399=