Canonical Allele Identifier: CA1143715978
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684226A= , CM000663.2:g.114684226A= GRCh38
NC_000001.10:g.115226847A= , CM000663.1:g.115226847A= GRCh37
NC_000001.9:g.115028370A= NCBI36
NG_008012.1:g.16330T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.508T= ENSP00000358551.4:p.Trp170=
ENST00000520113.7:c.520T= MANE Select ENSP00000430075.3:p.Trp174=
ENST00000637080.1:c.523T= ENSP00000489753.1:p.Trp175=
ENST00000639077.1:n.185T=
ENST00000369538.3:c.607T= ENSP00000358551.3:p.Trp203=
ENST00000485564.3:n.394T=
ENST00000520113.6:c.619T= ENSP00000430075.2:p.Trp207=
NM_000036.2:c.619T= NP_000027.2:p.Trp207=
NM_001172626.1:c.607T= NP_001166097.1:p.Trp203=
NM_000036.3:c.520T= MANE Select NP_000027.3:p.Trp174=
NM_001172626.2:c.508T= NP_001166097.2:p.Trp170=