Canonical Allele Identifier: CA1190281759

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684225C= , CM000663.2:g.114684225C=	GRCh38
NC_000001.10:g.115226846C= , CM000663.1:g.115226846C=	GRCh37
NC_000001.9:g.115028369C=	NCBI36
NG_008012.1:g.16331G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.509G=	ENSP00000358551.4:p.Trp170=
ENST00000520113.7:c.521G= MANE Select	ENSP00000430075.3:p.Trp174=
ENST00000637080.1:c.524G=	ENSP00000489753.1:p.Trp175=
ENST00000639077.1:n.186G=
ENST00000369538.3:c.608G=	ENSP00000358551.3:p.Trp203=
ENST00000485564.3:n.395G=
ENST00000520113.6:c.620G=	ENSP00000430075.2:p.Trp207=
NM_000036.2:c.620G=	NP_000027.2:p.Trp207=
NM_001172626.1:c.608G=	NP_001166097.1:p.Trp203=
NM_000036.3:c.521G= MANE Select	NP_000027.3:p.Trp174=
NM_001172626.2:c.509G=	NP_001166097.2:p.Trp170=