Canonical Allele Identifier: CA1145586458
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684200T= , CM000663.2:g.114684200T= GRCh38
NC_000001.10:g.115226821T= , CM000663.1:g.115226821T= GRCh37
NC_000001.9:g.115028344T= NCBI36
NG_008012.1:g.16356A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.534A= ENSP00000358551.4:p.Pro178=
ENST00000520113.7:c.546A= MANE Select ENSP00000430075.3:p.Pro182=
ENST00000637080.1:c.549A= ENSP00000489753.1:p.Pro183=
ENST00000639077.1:n.211A=
ENST00000369538.3:c.633A= ENSP00000358551.3:p.Pro211=
ENST00000485564.3:n.420A=
ENST00000520113.6:c.645A= ENSP00000430075.2:p.Pro215=
NM_000036.2:c.645A= NP_000027.2:p.Pro215=
NM_001172626.1:c.633A= NP_001166097.1:p.Pro211=
NM_000036.3:c.546A= MANE Select NP_000027.3:p.Pro182=
NM_001172626.2:c.534A= NP_001166097.2:p.Pro178=