Canonical Allele Identifier: CA1144010467

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684242G= , CM000663.2:g.114684242G=	GRCh38
NC_000001.10:g.115226863G= , CM000663.1:g.115226863G=	GRCh37
NC_000001.9:g.115028386G=	NCBI36
NG_008012.1:g.16314C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.492C=	ENSP00000358551.4:p.Asn164=
ENST00000520113.7:c.504C= MANE Select	ENSP00000430075.3:p.Asn168=
ENST00000637080.1:c.507C=	ENSP00000489753.1:p.Asn169=
ENST00000639077.1:n.169C=
ENST00000369538.3:c.591C=	ENSP00000358551.3:p.Asn197=
ENST00000485564.3:n.378C=
ENST00000520113.6:c.603C=	ENSP00000430075.2:p.Asn201=
NM_000036.2:c.603C=	NP_000027.2:p.Asn201=
NM_001172626.1:c.591C=	NP_001166097.1:p.Asn197=
NM_000036.3:c.504C= MANE Select	NP_000027.3:p.Asn168=
NM_001172626.2:c.492C=	NP_001166097.2:p.Asn164=