Canonical Allele Identifier: CA1190282017
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684376A= , CM000663.2:g.114684376A= GRCh38
NC_000001.10:g.115226997A= , CM000663.1:g.115226997A= GRCh37
NC_000001.9:g.115028520A= NCBI36
NG_008012.1:g.16180T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.370-12T= ENSP00000358551.4:n.370-12T=
ENST00000520113.7:c.382-12T= MANE Select ENSP00000430075.3:n.382-12T=
ENST00000637080.1:c.385-12T= ENSP00000489753.1:n.385-12T=
ENST00000639077.1:n.47-12T=
ENST00000369538.3:c.469-12T= ENSP00000358551.3:n.469-12T=
ENST00000485564.3:n.256-12T=
ENST00000520113.6:c.481-12T= ENSP00000430075.2:n.481-12T=
NM_000036.2:c.481-12T= NP_000027.2:n.481-12T=
NM_001172626.1:c.469-12T= NP_001166097.1:n.469-12T=
NM_000036.3:c.382-12T= MANE Select NP_000027.3:n.382-12T=
NM_001172626.2:c.370-12T= NP_001166097.2:n.370-12T=