Canonical Allele Identifier: CA1146335914
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677992G= , CM000663.2:g.114677992G= GRCh38
NC_000001.10:g.115220613G= , CM000663.1:g.115220613G= GRCh37
NC_000001.9:g.115022136G= NCBI36
NG_008012.1:g.22564C=

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1130C= ENSP00000358551.4:p.Pro377=
ENST00000520113.7:c.1142C= MANE Select ENSP00000430075.3:p.Pro381=
ENST00000637080.1:c.925C= ENSP00000489753.1:n.925C=
ENST00000639077.1:n.807C=
ENST00000369538.3:c.1229C= ENSP00000358551.3:p.Pro410=
ENST00000520113.6:c.1241C= ENSP00000430075.2:p.Pro414=
NM_000036.2:c.1241C= NP_000027.2:p.Pro414=
NM_001172626.1:c.1229C= NP_001166097.1:p.Pro410=
NM_000036.3:c.1142C= MANE Select NP_000027.3:p.Pro381=
NM_001172626.2:c.1130C= NP_001166097.2:p.Pro377=