Canonical Allele Identifier: CA1190281835
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684275C= , CM000663.2:g.114684275C= GRCh38
NC_000001.10:g.115226896C= , CM000663.1:g.115226896C= GRCh37
NC_000001.9:g.115028419C= NCBI36
NG_008012.1:g.16281G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.459G= ENSP00000358551.4:p.Arg153=
ENST00000520113.7:c.471G= MANE Select ENSP00000430075.3:p.Arg157=
ENST00000637080.1:c.474G= ENSP00000489753.1:p.Arg158=
ENST00000639077.1:n.136G=
ENST00000369538.3:c.558G= ENSP00000358551.3:p.Arg186=
ENST00000485564.3:n.345G=
ENST00000520113.6:c.570G= ENSP00000430075.2:p.Arg190=
NM_000036.2:c.570G= NP_000027.2:p.Arg190=
NM_001172626.1:c.558G= NP_001166097.1:p.Arg186=
NM_000036.3:c.471G= MANE Select NP_000027.3:p.Arg157=
NM_001172626.2:c.459G= NP_001166097.2:p.Arg153=