Canonical Allele Identifier: CA1190281737
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684208A= , CM000663.2:g.114684208A= GRCh38
NC_000001.10:g.115226829A= , CM000663.1:g.115226829A= GRCh37
NC_000001.9:g.115028352A= NCBI36
NG_008012.1:g.16348T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.526T= ENSP00000358551.4:p.Phe176=
ENST00000520113.7:c.538T= MANE Select ENSP00000430075.3:p.Phe180=
ENST00000637080.1:c.541T= ENSP00000489753.1:p.Phe181=
ENST00000639077.1:n.203T=
ENST00000369538.3:c.625T= ENSP00000358551.3:p.Phe209=
ENST00000485564.3:n.412T=
ENST00000520113.6:c.637T= ENSP00000430075.2:p.Phe213=
NM_000036.2:c.637T= NP_000027.2:p.Phe213=
NM_001172626.1:c.625T= NP_001166097.1:p.Phe209=
NM_000036.3:c.538T= MANE Select NP_000027.3:p.Phe180=
NM_001172626.2:c.526T= NP_001166097.2:p.Phe176=