Canonical Allele Identifier: CA1190281857
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684285G= , CM000663.2:g.114684285G= GRCh38
NC_000001.10:g.115226906G= , CM000663.1:g.115226906G= GRCh37
NC_000001.9:g.115028429G= NCBI36
NG_008012.1:g.16271C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.449C= ENSP00000358551.4:p.Ser150=
ENST00000520113.7:c.461C= MANE Select ENSP00000430075.3:p.Ser154=
ENST00000637080.1:c.464C= ENSP00000489753.1:p.Ser155=
ENST00000639077.1:n.126C=
ENST00000369538.3:c.548C= ENSP00000358551.3:p.Ser183=
ENST00000485564.3:n.335C=
ENST00000520113.6:c.560C= ENSP00000430075.2:p.Ser187=
NM_000036.2:c.560C= NP_000027.2:p.Ser187=
NM_001172626.1:c.548C= NP_001166097.1:p.Ser183=
NM_000036.3:c.461C= MANE Select NP_000027.3:p.Ser154=
NM_001172626.2:c.449C= NP_001166097.2:p.Ser150=