Canonical Allele Identifier: CA1146374834
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677980C= , CM000663.2:g.114677980C= GRCh38
NC_000001.10:g.115220601C= , CM000663.1:g.115220601C= GRCh37
NC_000001.9:g.115022124C= NCBI36
NG_008012.1:g.22576G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1142G= ENSP00000358551.4:p.Ser381=
ENST00000520113.7:c.1154G= MANE Select ENSP00000430075.3:p.Ser385=
ENST00000637080.1:c.937G= ENSP00000489753.1:n.937G=
ENST00000639077.1:n.819G=
ENST00000369538.3:c.1241G= ENSP00000358551.3:p.Ser414=
ENST00000520113.6:c.1253G= ENSP00000430075.2:p.Ser418=
NM_000036.2:c.1253G= NP_000027.2:p.Ser418=
NM_001172626.1:c.1241G= NP_001166097.1:p.Ser414=
NM_000036.3:c.1154G= MANE Select NP_000027.3:p.Ser385=
NM_001172626.2:c.1142G= NP_001166097.2:p.Ser381=