Canonical Allele Identifier: CA1190288149
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693454G= , CM000663.2:g.114693454G= GRCh38
NC_000001.10:g.115236075G= , CM000663.1:g.115236075G= GRCh37
NC_000001.9:g.115037598G= NCBI36
NG_008012.1:g.7102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.22+1996C= ENSP00000358551.4:n.22+1996C=
ENST00000520113.7:c.23-7C= MANE Select ENSP00000430075.3:n.23-7C=
ENST00000637080.1:c.37+1983C= ENSP00000489753.1:n.37+1983C=
ENST00000369538.3:c.121+1996C= ENSP00000358551.3:n.121+1996C=
ENST00000520113.6:c.122-7C= ENSP00000430075.2:n.122-7C=
NM_000036.2:c.122-7C= NP_000027.2:n.122-7C=
NM_001172626.1:c.121+1996C= NP_001166097.1:n.121+1996C=
NM_000036.3:c.23-7C= MANE Select NP_000027.3:n.23-7C=
NM_001172626.2:c.22+1996C= NP_001166097.2:n.22+1996C=