Canonical Allele Identifier: CA341748973
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677925A>T , CM000663.2:g.114677925A>T GRCh38
NC_000001.10:g.115220546A>T , CM000663.1:g.115220546A>T GRCh37
NC_000001.9:g.115022069A>T NCBI36
NG_008012.1:g.22631T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1197T>A ENSP00000358551.4:p.Phe399Leu
ENST00000520113.7:c.1209T>A MANE Select ENSP00000430075.3:p.Phe403Leu
ENST00000637080.1:c.992T>A ENSP00000489753.1:n.992T>A
ENST00000639077.1:n.874T>A
ENST00000369538.3:c.1296T>A ENSP00000358551.3:p.Phe432Leu
ENST00000520113.6:c.1308T>A ENSP00000430075.2:p.Phe436Leu
NM_000036.2:c.1308T>A NP_000027.2:p.Phe436Leu
NM_001172626.1:c.1296T>A NP_001166097.1:p.Phe432Leu
NM_000036.3:c.1209T>A MANE Select NP_000027.3:p.Phe403Leu
NM_001172626.2:c.1197T>A NP_001166097.2:p.Phe399Leu