Canonical Allele Identifier: CA1190276394
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677678A= , CM000663.2:g.114677678A= GRCh38
NC_000001.10:g.115220299A= , CM000663.1:g.115220299A= GRCh37
NC_000001.9:g.115021822A= NCBI36
NG_008012.1:g.22878T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1213-164T= ENSP00000358551.4:n.1213-164T=
ENST00000520113.7:c.1225-164T= MANE Select ENSP00000430075.3:n.1225-164T=
ENST00000637080.1:c.1008-164T= ENSP00000489753.1:n.1008-164T=
ENST00000639077.1:n.890-164T=
ENST00000369538.3:c.1312-164T= ENSP00000358551.3:n.1312-164T=
ENST00000520113.6:c.1324-164T= ENSP00000430075.2:n.1324-164T=
NM_000036.2:c.1324-164T= NP_000027.2:n.1324-164T=
NM_001172626.1:c.1312-164T= NP_001166097.1:n.1312-164T=
NM_000036.3:c.1225-164T= MANE Select NP_000027.3:n.1225-164T=
NM_001172626.2:c.1213-164T= NP_001166097.2:n.1213-164T=