Canonical Allele Identifier: CA1190277194
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114679429T= , CM000663.2:g.114679429T= GRCh38
NC_000001.10:g.115222050T= , CM000663.1:g.115222050T= GRCh37
NC_000001.9:g.115023573T= NCBI36
NG_008012.1:g.21127A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.885+150A= ENSP00000358551.4:n.885+150A=
ENST00000520113.7:c.897+150A= MANE Select ENSP00000430075.3:n.897+150A=
ENST00000637080.1:c.680+150A= ENSP00000489753.1:n.680+150A=
ENST00000639077.1:n.562+150A=
ENST00000369538.3:c.984+150A= ENSP00000358551.3:n.984+150A=
ENST00000520113.6:c.996+150A= ENSP00000430075.2:n.996+150A=
NM_000036.2:c.996+150A= NP_000027.2:n.996+150A=
NM_001172626.1:c.984+150A= NP_001166097.1:n.984+150A=
NM_000036.3:c.897+150A= MANE Select NP_000027.3:n.897+150A=
NM_001172626.2:c.885+150A= NP_001166097.2:n.885+150A=