Canonical Allele Identifier: CA1190281802

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684241T= , CM000663.2:g.114684241T=	GRCh38
NC_000001.10:g.115226862T= , CM000663.1:g.115226862T=	GRCh37
NC_000001.9:g.115028385T=	NCBI36
NG_008012.1:g.16315A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.493A=	ENSP00000358551.4:p.Ile165=
ENST00000520113.7:c.505A= MANE Select	ENSP00000430075.3:p.Ile169=
ENST00000637080.1:c.508A=	ENSP00000489753.1:p.Ile170=
ENST00000639077.1:n.170A=
ENST00000369538.3:c.592A=	ENSP00000358551.3:p.Ile198=
ENST00000485564.3:n.379A=
ENST00000520113.6:c.604A=	ENSP00000430075.2:p.Ile202=
NM_000036.2:c.604A=	NP_000027.2:p.Ile202=
NM_001172626.1:c.592A=	NP_001166097.1:p.Ile198=
NM_000036.3:c.505A= MANE Select	NP_000027.3:p.Ile169=
NM_001172626.2:c.493A=	NP_001166097.2:p.Ile165=