Canonical Allele Identifier: CA2647247477
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677766dup , CM000663.2:g.114677766dup GRCh38
NC_000001.10:g.115220387dup , CM000663.1:g.115220387dup GRCh37
NC_000001.9:g.115021910dup NCBI36
NG_008012.1:g.22792dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1212+146dup ENSP00000358551.4:n.1212+146dup
ENST00000520113.7:c.1224+146dup MANE Select ENSP00000430075.3:n.1224+146dup
ENST00000637080.1:c.1007+146dup ENSP00000489753.1:n.1007+146dup
ENST00000639077.1:n.889+146dup
ENST00000369538.3:c.1311+146dup ENSP00000358551.3:n.1311+146dup
ENST00000520113.6:c.1323+146dup ENSP00000430075.2:n.1323+146dup
NM_000036.2:c.1323+146dup NP_000027.2:n.1323+146dup
NM_001172626.1:c.1311+146dup NP_001166097.1:n.1311+146dup
NM_000036.3:c.1224+146dup MANE Select NP_000027.3:n.1224+146dup
NM_001172626.2:c.1212+146dup NP_001166097.2:n.1212+146dup