Canonical Allele Identifier: CA1140726232
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114678495C= , CM000663.2:g.114678495C= GRCh38
NC_000001.10:g.115221116C= , CM000663.1:g.115221116C= GRCh37
NC_000001.9:g.115022639C= NCBI36
NG_008012.1:g.22061G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.918G= ENSP00000358551.4:p.Met306=
ENST00000520113.7:c.930G= MANE Select ENSP00000430075.3:p.Met310=
ENST00000637080.1:c.713G= ENSP00000489753.1:n.713G=
ENST00000639077.1:n.595G=
ENST00000369538.3:c.1017G= ENSP00000358551.3:p.Met339=
ENST00000520113.6:c.1029G= ENSP00000430075.2:p.Met343=
NM_000036.2:c.1029G= NP_000027.2:p.Met343=
NM_001172626.1:c.1017G= NP_001166097.1:p.Met339=
NM_000036.3:c.930G= MANE Select NP_000027.3:p.Met310=
NM_001172626.2:c.918G= NP_001166097.2:p.Met306=