Canonical Allele Identifier: CA1190281907
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684313A= , CM000663.2:g.114684313A= GRCh38
NC_000001.10:g.115226934A= , CM000663.1:g.115226934A= GRCh37
NC_000001.9:g.115028457A= NCBI36
NG_008012.1:g.16243T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.421T= ENSP00000358551.4:p.Cys141=
ENST00000520113.7:c.433T= MANE Select ENSP00000430075.3:p.Cys145=
ENST00000637080.1:c.436T= ENSP00000489753.1:p.Cys146=
ENST00000639077.1:n.98T=
ENST00000369538.3:c.520T= ENSP00000358551.3:p.Cys174=
ENST00000485564.3:n.307T=
ENST00000520113.6:c.532T= ENSP00000430075.2:p.Cys178=
NM_000036.2:c.532T= NP_000027.2:p.Cys178=
NM_001172626.1:c.520T= NP_001166097.1:p.Cys174=
NM_000036.3:c.433T= MANE Select NP_000027.3:p.Cys145=
NM_001172626.2:c.421T= NP_001166097.2:p.Cys141=