Canonical Allele Identifier: CA1141580998
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677465C= , CM000663.2:g.114677465C= GRCh38
NC_000001.10:g.115220086C= , CM000663.1:g.115220086C= GRCh37
NC_000001.9:g.115021609C= NCBI36
NG_008012.1:g.23091G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1262G= ENSP00000358551.4:p.Arg421=
ENST00000520113.7:c.1274G= MANE Select ENSP00000430075.3:p.Arg425=
ENST00000637080.1:c.1057G= ENSP00000489753.1:n.1057G=
ENST00000639077.1:n.939G=
ENST00000369538.3:c.1361G= ENSP00000358551.3:p.Arg454=
ENST00000520113.6:c.1373G= ENSP00000430075.2:p.Arg458=
NM_000036.2:c.1373G= NP_000027.2:p.Arg458=
NM_001172626.1:c.1361G= NP_001166097.1:p.Arg454=
NM_000036.3:c.1274G= MANE Select NP_000027.3:p.Arg425=
NM_001172626.2:c.1262G= NP_001166097.2:p.Arg421=