Canonical Allele Identifier: CA1190288138
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693437T= , CM000663.2:g.114693437T= GRCh38
NC_000001.10:g.115236058T= , CM000663.1:g.115236058T= GRCh37
NC_000001.9:g.115037581T= NCBI36
NG_008012.1:g.7119A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.22+2013A= ENSP00000358551.4:n.22+2013A=
ENST00000520113.7:c.33A= MANE Select ENSP00000430075.3:p.Lys11=
ENST00000637080.1:c.37+2000A= ENSP00000489753.1:n.37+2000A=
ENST00000369538.3:c.121+2013A= ENSP00000358551.3:n.121+2013A=
ENST00000520113.6:c.132A= ENSP00000430075.2:p.Lys44=
NM_000036.2:c.132A= NP_000027.2:p.Lys44=
NM_001172626.1:c.121+2013A= NP_001166097.1:n.121+2013A=
NM_000036.3:c.33A= MANE Select NP_000027.3:p.Lys11=
NM_001172626.2:c.22+2013A= NP_001166097.2:n.22+2013A=