Canonical Allele Identifier: CA1190281872
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684297T= , CM000663.2:g.114684297T= GRCh38
NC_000001.10:g.115226918T= , CM000663.1:g.115226918T= GRCh37
NC_000001.9:g.115028441T= NCBI36
NG_008012.1:g.16259A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.437A= ENSP00000358551.4:p.Tyr146=
ENST00000520113.7:c.449A= MANE Select ENSP00000430075.3:p.Tyr150=
ENST00000637080.1:c.452A= ENSP00000489753.1:p.Tyr151=
ENST00000639077.1:n.114A=
ENST00000369538.3:c.536A= ENSP00000358551.3:p.Tyr179=
ENST00000485564.3:n.323A=
ENST00000520113.6:c.548A= ENSP00000430075.2:p.Tyr183=
NM_000036.2:c.548A= NP_000027.2:p.Tyr183=
NM_001172626.1:c.536A= NP_001166097.1:p.Tyr179=
NM_000036.3:c.449A= MANE Select NP_000027.3:p.Tyr150=
NM_001172626.2:c.437A= NP_001166097.2:p.Tyr146=