Canonical Allele Identifier: CA1190281695

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684184T= , CM000663.2:g.114684184T=	GRCh38
NC_000001.10:g.115226805T= , CM000663.1:g.115226805T=	GRCh37
NC_000001.9:g.115028328T=	NCBI36
NG_008012.1:g.16372A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.535+15A=	ENSP00000358551.4:n.535+15A=
ENST00000520113.7:c.547+15A= MANE Select	ENSP00000430075.3:n.547+15A=
ENST00000637080.1:c.550+15A=	ENSP00000489753.1:n.550+15A=
ENST00000639077.1:n.212+15A=
ENST00000369538.3:c.634+15A=	ENSP00000358551.3:n.634+15A=
ENST00000485564.3:n.421+15A=
ENST00000520113.6:c.646+15A=	ENSP00000430075.2:n.646+15A=
NM_000036.2:c.646+15A=	NP_000027.2:n.646+15A=
NM_001172626.1:c.634+15A=	NP_001166097.1:n.634+15A=
NM_000036.3:c.547+15A= MANE Select	NP_000027.3:n.547+15A=
NM_001172626.2:c.535+15A=	NP_001166097.2:n.535+15A=