Canonical Allele Identifier: CA2574035136
Gene: AMPD1 HGNC NCBI

Linked Data

gnomAD v4: 1-114677611-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677611A>T , CM000663.2:g.114677611A>T GRCh38
NC_000001.10:g.115220232A>T , CM000663.1:g.115220232A>T GRCh37
NC_000001.9:g.115021755A>T NCBI36
NG_008012.1:g.22945T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1213-97T>A ENSP00000358551.4:n.1213-97T>A
ENST00000520113.7:c.1225-97T>A MANE Select ENSP00000430075.3:n.1225-97T>A
ENST00000637080.1:c.1008-97T>A ENSP00000489753.1:n.1008-97T>A
ENST00000639077.1:n.890-97T>A
ENST00000369538.3:c.1312-97T>A ENSP00000358551.3:n.1312-97T>A
ENST00000520113.6:c.1324-97T>A ENSP00000430075.2:n.1324-97T>A
NM_000036.2:c.1324-97T>A NP_000027.2:n.1324-97T>A
NM_001172626.1:c.1312-97T>A NP_001166097.1:n.1312-97T>A
NM_000036.3:c.1225-97T>A MANE Select NP_000027.3:n.1225-97T>A
NM_001172626.2:c.1213-97T>A NP_001166097.2:n.1213-97T>A
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