Canonical Allele Identifier: CA1190281877
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684298A= , CM000663.2:g.114684298A= GRCh38
NC_000001.10:g.115226919A= , CM000663.1:g.115226919A= GRCh37
NC_000001.9:g.115028442A= NCBI36
NG_008012.1:g.16258T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.436T= ENSP00000358551.4:p.Tyr146=
ENST00000520113.7:c.448T= MANE Select ENSP00000430075.3:p.Tyr150=
ENST00000637080.1:c.451T= ENSP00000489753.1:p.Tyr151=
ENST00000639077.1:n.113T=
ENST00000369538.3:c.535T= ENSP00000358551.3:p.Tyr179=
ENST00000485564.3:n.322T=
ENST00000520113.6:c.547T= ENSP00000430075.2:p.Tyr183=
NM_000036.2:c.547T= NP_000027.2:p.Tyr183=
NM_001172626.1:c.535T= NP_001166097.1:p.Tyr179=
NM_000036.3:c.448T= MANE Select NP_000027.3:p.Tyr150=
NM_001172626.2:c.436T= NP_001166097.2:p.Tyr146=