Canonical Allele Identifier: CA1145410829
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684239A= , CM000663.2:g.114684239A= GRCh38
NC_000001.10:g.115226860A= , CM000663.1:g.115226860A= GRCh37
NC_000001.9:g.115028383A= NCBI36
NG_008012.1:g.16317T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.495T= ENSP00000358551.4:p.Ile165=
ENST00000520113.7:c.507T= MANE Select ENSP00000430075.3:p.Ile169=
ENST00000637080.1:c.510T= ENSP00000489753.1:p.Ile170=
ENST00000639077.1:n.172T=
ENST00000369538.3:c.594T= ENSP00000358551.3:p.Ile198=
ENST00000485564.3:n.381T=
ENST00000520113.6:c.606T= ENSP00000430075.2:p.Ile202=
NM_000036.2:c.606T= NP_000027.2:p.Ile202=
NM_001172626.1:c.594T= NP_001166097.1:p.Ile198=
NM_000036.3:c.507T= MANE Select NP_000027.3:p.Ile169=
NM_001172626.2:c.495T= NP_001166097.2:p.Ile165=