Canonical Allele Identifier: CA1190277317
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114679558C= , CM000663.2:g.114679558C= GRCh38
NC_000001.10:g.115222179C= , CM000663.1:g.115222179C= GRCh37
NC_000001.9:g.115023702C= NCBI36
NG_008012.1:g.20998G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.885+21G= ENSP00000358551.4:n.885+21G=
ENST00000520113.7:c.897+21G= MANE Select ENSP00000430075.3:n.897+21G=
ENST00000637080.1:c.680+21G= ENSP00000489753.1:n.680+21G=
ENST00000639077.1:n.562+21G=
ENST00000369538.3:c.984+21G= ENSP00000358551.3:n.984+21G=
ENST00000520113.6:c.996+21G= ENSP00000430075.2:n.996+21G=
NM_000036.2:c.996+21G= NP_000027.2:n.996+21G=
NM_001172626.1:c.984+21G= NP_001166097.1:n.984+21G=
NM_000036.3:c.897+21G= MANE Select NP_000027.3:n.897+21G=
NM_001172626.2:c.885+21G= NP_001166097.2:n.885+21G=