Canonical Allele Identifier: CA1190281701
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684187G= , CM000663.2:g.114684187G= GRCh38
NC_000001.10:g.115226808G= , CM000663.1:g.115226808G= GRCh37
NC_000001.9:g.115028331G= NCBI36
NG_008012.1:g.16369C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.535+12C= ENSP00000358551.4:n.535+12C=
ENST00000520113.7:c.547+12C= MANE Select ENSP00000430075.3:n.547+12C=
ENST00000637080.1:c.550+12C= ENSP00000489753.1:n.550+12C=
ENST00000639077.1:n.212+12C=
ENST00000369538.3:c.634+12C= ENSP00000358551.3:n.634+12C=
ENST00000485564.3:n.421+12C=
ENST00000520113.6:c.646+12C= ENSP00000430075.2:n.646+12C=
NM_000036.2:c.646+12C= NP_000027.2:n.646+12C=
NM_001172626.1:c.634+12C= NP_001166097.1:n.634+12C=
NM_000036.3:c.547+12C= MANE Select NP_000027.3:n.547+12C=
NM_001172626.2:c.535+12C= NP_001166097.2:n.535+12C=