Canonical Allele Identifier: CA1190282147
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684486C= , CM000663.2:g.114684486C= GRCh38
NC_000001.10:g.115227107C= , CM000663.1:g.115227107C= GRCh37
NC_000001.9:g.115028630C= NCBI36
NG_008012.1:g.16070G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.370-122G= ENSP00000358551.4:n.370-122G=
ENST00000520113.7:c.382-122G= MANE Select ENSP00000430075.3:n.382-122G=
ENST00000637080.1:c.385-122G= ENSP00000489753.1:n.385-122G=
ENST00000639077.1:n.4G=
ENST00000369538.3:c.469-122G= ENSP00000358551.3:n.469-122G=
ENST00000485564.3:n.256-122G=
ENST00000520113.6:c.481-122G= ENSP00000430075.2:n.481-122G=
NM_000036.2:c.481-122G= NP_000027.2:n.481-122G=
NM_001172626.1:c.469-122G= NP_001166097.1:n.469-122G=
NM_000036.3:c.382-122G= MANE Select NP_000027.3:n.382-122G=
NM_001172626.2:c.370-122G= NP_001166097.2:n.370-122G=