Canonical Allele Identifier: CA341749095
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677978C>G , CM000663.2:g.114677978C>G GRCh38
NC_000001.10:g.115220599C>G , CM000663.1:g.115220599C>G GRCh37
NC_000001.9:g.115022122C>G NCBI36
NG_008012.1:g.22578G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1144G>C ENSP00000358551.4:p.Glu382Gln
ENST00000520113.7:c.1156G>C MANE Select ENSP00000430075.3:p.Glu386Gln
ENST00000637080.1:n.939G>C ENSP00000489753.1:n.939G>C
ENST00000639077.1:n.821G>C
ENST00000369538.3:c.1243G>C ENSP00000358551.3:p.Glu415Gln
ENST00000520113.6:c.1255G>C ENSP00000430075.2:p.Glu419Gln
NM_000036.2:c.1255G>C NP_000027.2:p.Glu419Gln
NM_001172626.1:c.1243G>C NP_001166097.1:p.Glu415Gln
NM_000036.3:c.1156G>C MANE Select NP_000027.3:p.Glu386Gln
NM_001172626.2:c.1144G>C NP_001166097.2:p.Glu382Gln