Canonical Allele Identifier: CA1140472733
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114693436G= , CM000663.2:g.114693436G= GRCh38
NC_000001.10:g.115236057G= , CM000663.1:g.115236057G= GRCh37
NC_000001.9:g.115037580G= NCBI36
NG_008012.1:g.7120C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.22+2014C= ENSP00000358551.4:n.22+2014C=
ENST00000520113.7:c.34C= MANE Select ENSP00000430075.3:p.Gln12=
ENST00000637080.1:c.37+2001C= ENSP00000489753.1:n.37+2001C=
ENST00000369538.3:c.121+2014C= ENSP00000358551.3:n.121+2014C=
ENST00000520113.6:c.133C= ENSP00000430075.2:p.Gln45=
NM_000036.2:c.133C= NP_000027.2:p.Gln45=
NM_001172626.1:c.121+2014C= NP_001166097.1:n.121+2014C=
NM_000036.3:c.34C= MANE Select NP_000027.3:p.Gln12=
NM_001172626.2:c.22+2014C= NP_001166097.2:n.22+2014C=