Canonical Allele Identifier: CA2647253105
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684120A>T , CM000663.2:g.114684120A>T GRCh38
NC_000001.10:g.115226741A>T , CM000663.1:g.115226741A>T GRCh37
NC_000001.9:g.115028264A>T NCBI36
NG_008012.1:g.16436T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.535+79T>A ENSP00000358551.4:n.535+79T>A
ENST00000520113.7:c.547+79T>A MANE Select ENSP00000430075.3:n.547+79T>A
ENST00000637080.1:c.550+79T>A ENSP00000489753.1:n.550+79T>A
ENST00000639077.1:n.212+79T>A
ENST00000369538.3:c.634+79T>A ENSP00000358551.3:n.634+79T>A
ENST00000485564.3:n.421+79T>A
ENST00000520113.6:c.646+79T>A ENSP00000430075.2:n.646+79T>A
NM_000036.2:c.646+79T>A NP_000027.2:n.646+79T>A
NM_001172626.1:c.634+79T>A NP_001166097.1:n.634+79T>A
NM_000036.3:c.547+79T>A MANE Select NP_000027.3:n.547+79T>A
NM_001172626.2:c.535+79T>A NP_001166097.2:n.535+79T>A