Canonical Allele Identifier: CA1190276287
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677402T= , CM000663.2:g.114677402T= GRCh38
NC_000001.10:g.115220023T= , CM000663.1:g.115220023T= GRCh37
NC_000001.9:g.115021546T= NCBI36
NG_008012.1:g.23154A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1325A= ENSP00000358551.4:p.Asn442=
ENST00000520113.7:c.1337A= MANE Select ENSP00000430075.3:p.Asn446=
ENST00000637080.1:c.1120A= ENSP00000489753.1:n.1120A=
ENST00000639077.1:n.1002A=
ENST00000369538.3:c.1424A= ENSP00000358551.3:p.Asn475=
ENST00000520113.6:c.1436A= ENSP00000430075.2:p.Asn479=
NM_000036.2:c.1436A= NP_000027.2:p.Asn479=
NM_001172626.1:c.1424A= NP_001166097.1:p.Asn475=
NM_000036.3:c.1337A= MANE Select NP_000027.3:p.Asn446=
NM_001172626.2:c.1325A= NP_001166097.2:p.Asn442=