Canonical Allele Identifier: CA1190281757
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114684224C= , CM000663.2:g.114684224C= GRCh38
NC_000001.10:g.115226845C= , CM000663.1:g.115226845C= GRCh37
NC_000001.9:g.115028368C= NCBI36
NG_008012.1:g.16332G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.510G= ENSP00000358551.4:p.Trp170=
ENST00000520113.7:c.522G= MANE Select ENSP00000430075.3:p.Trp174=
ENST00000637080.1:c.525G= ENSP00000489753.1:p.Trp175=
ENST00000639077.1:n.187G=
ENST00000369538.3:c.609G= ENSP00000358551.3:p.Trp203=
ENST00000485564.3:n.396G=
ENST00000520113.6:c.621G= ENSP00000430075.2:p.Trp207=
NM_000036.2:c.621G= NP_000027.2:p.Trp207=
NM_001172626.1:c.609G= NP_001166097.1:p.Trp203=
NM_000036.3:c.522G= MANE Select NP_000027.3:p.Trp174=
NM_001172626.2:c.510G= NP_001166097.2:p.Trp170=