Canonical Allele Identifier: CA2647256205
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693342G>A , CM000663.2:g.114693342G>A GRCh38
NC_000001.10:g.115235963G>A , CM000663.1:g.115235963G>A GRCh37
NC_000001.9:g.115037486G>A NCBI36
NG_008012.1:g.7214C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.22+2108C>T ENSP00000358551.4:n.22+2108C>T
ENST00000520113.7:c.34+94C>T MANE Select ENSP00000430075.3:n.34+94C>T
ENST00000637080.1:c.37+2095C>T ENSP00000489753.1:n.37+2095C>T
ENST00000369538.3:c.121+2108C>T ENSP00000358551.3:n.121+2108C>T
ENST00000520113.6:c.133+94C>T ENSP00000430075.2:n.133+94C>T
NM_000036.2:c.133+94C>T NP_000027.2:n.133+94C>T
NM_001172626.1:c.121+2108C>T NP_001166097.1:n.121+2108C>T
NM_000036.3:c.34+94C>T MANE Select NP_000027.3:n.34+94C>T
NM_001172626.2:c.22+2108C>T NP_001166097.2:n.22+2108C>T