Canonical Allele Identifier: CA1190288096
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693321G= , CM000663.2:g.114693321G= GRCh38
NC_000001.10:g.115235942G= , CM000663.1:g.115235942G= GRCh37
NC_000001.9:g.115037465G= NCBI36
NG_008012.1:g.7235C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.22+2129C= ENSP00000358551.4:n.22+2129C=
ENST00000520113.7:c.34+115C= MANE Select ENSP00000430075.3:n.34+115C=
ENST00000637080.1:c.37+2116C= ENSP00000489753.1:n.37+2116C=
ENST00000369538.3:c.121+2129C= ENSP00000358551.3:n.121+2129C=
ENST00000520113.6:c.133+115C= ENSP00000430075.2:n.133+115C=
NM_000036.2:c.133+115C= NP_000027.2:n.133+115C=
NM_001172626.1:c.121+2129C= NP_001166097.1:n.121+2129C=
NM_000036.3:c.34+115C= MANE Select NP_000027.3:n.34+115C=
NM_001172626.2:c.22+2129C= NP_001166097.2:n.22+2129C=