Canonical Allele Identifier: CA1143611302
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684246C= , CM000663.2:g.114684246C= GRCh38
NC_000001.10:g.115226867C= , CM000663.1:g.115226867C= GRCh37
NC_000001.9:g.115028390C= NCBI36
NG_008012.1:g.16310G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.488G= ENSP00000358551.4:p.Arg163=
ENST00000520113.7:c.500G= MANE Select ENSP00000430075.3:p.Arg167=
ENST00000637080.1:c.503G= ENSP00000489753.1:p.Arg168=
ENST00000639077.1:n.165G=
ENST00000369538.3:c.587G= ENSP00000358551.3:p.Arg196=
ENST00000485564.3:n.374G=
ENST00000520113.6:c.599G= ENSP00000430075.2:p.Arg200=
NM_000036.2:c.599G= NP_000027.2:p.Arg200=
NM_001172626.1:c.587G= NP_001166097.1:p.Arg196=
NM_000036.3:c.500G= MANE Select NP_000027.3:p.Arg167=
NM_001172626.2:c.488G= NP_001166097.2:p.Arg163=