Canonical Allele Identifier: CA1147283936
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114678002T= , CM000663.2:g.114678002T= GRCh38
NC_000001.10:g.115220623T= , CM000663.1:g.115220623T= GRCh37
NC_000001.9:g.115022146T= NCBI36
NG_008012.1:g.22554A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1120A= ENSP00000358551.4:p.Lys374=
ENST00000520113.7:c.1132A= MANE Select ENSP00000430075.3:p.Lys378=
ENST00000637080.1:c.915A= ENSP00000489753.1:n.915A=
ENST00000639077.1:n.797A=
ENST00000369538.3:c.1219A= ENSP00000358551.3:p.Lys407=
ENST00000520113.6:c.1231A= ENSP00000430075.2:p.Lys411=
NM_000036.2:c.1231A= NP_000027.2:p.Lys411=
NM_001172626.1:c.1219A= NP_001166097.1:p.Lys407=
NM_000036.3:c.1132A= MANE Select NP_000027.3:p.Lys378=
NM_001172626.2:c.1120A= NP_001166097.2:p.Lys374=