Canonical Allele Identifier: CA2647249035
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114679437del , CM000663.2:g.114679437del GRCh38
NC_000001.10:g.115222058del , CM000663.1:g.115222058del GRCh37
NC_000001.9:g.115023581del NCBI36
NG_008012.1:g.21120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.885+143del ENSP00000358551.4:n.885+143del
ENST00000520113.7:c.897+143del MANE Select ENSP00000430075.3:n.897+143del
ENST00000637080.1:c.680+143del ENSP00000489753.1:n.680+143del
ENST00000639077.1:n.562+143del
ENST00000369538.3:c.984+143del ENSP00000358551.3:n.984+143del
ENST00000520113.6:c.996+143del ENSP00000430075.2:n.996+143del
NM_000036.2:c.996+143del NP_000027.2:n.996+143del
NM_001172626.1:c.984+143del NP_001166097.1:n.984+143del
NM_000036.3:c.897+143del MANE Select NP_000027.3:n.897+143del
NM_001172626.2:c.885+143del NP_001166097.2:n.885+143del