Canonical Allele Identifier: CA1190282036
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684385A= , CM000663.2:g.114684385A= GRCh38
NC_000001.10:g.115227006A= , CM000663.1:g.115227006A= GRCh37
NC_000001.9:g.115028529A= NCBI36
NG_008012.1:g.16171T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.370-21T= ENSP00000358551.4:n.370-21T=
ENST00000520113.7:c.382-21T= MANE Select ENSP00000430075.3:n.382-21T=
ENST00000637080.1:c.385-21T= ENSP00000489753.1:n.385-21T=
ENST00000639077.1:n.47-21T=
ENST00000369538.3:c.469-21T= ENSP00000358551.3:n.469-21T=
ENST00000485564.3:n.256-21T=
ENST00000520113.6:c.481-21T= ENSP00000430075.2:n.481-21T=
NM_000036.2:c.481-21T= NP_000027.2:n.481-21T=
NM_001172626.1:c.469-21T= NP_001166097.1:n.469-21T=
NM_000036.3:c.382-21T= MANE Select NP_000027.3:n.382-21T=
NM_001172626.2:c.370-21T= NP_001166097.2:n.370-21T=