Canonical Allele Identifier: CA341749152
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114678005C>T , CM000663.2:g.114678005C>T GRCh38
NC_000001.10:g.115220626C>T , CM000663.1:g.115220626C>T GRCh37
NC_000001.9:g.115022149C>T NCBI36
NG_008012.1:g.22551G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1117G>A ENSP00000358551.4:p.Asp373Asn
ENST00000520113.7:c.1129G>A MANE Select ENSP00000430075.3:p.Asp377Asn
ENST00000637080.1:c.912G>A ENSP00000489753.1:n.912G>A
ENST00000639077.1:n.794G>A
ENST00000369538.3:c.1216G>A ENSP00000358551.3:p.Asp406Asn
ENST00000520113.6:c.1228G>A ENSP00000430075.2:p.Asp410Asn
NM_000036.2:c.1228G>A NP_000027.2:p.Asp410Asn
NM_001172626.1:c.1216G>A NP_001166097.1:p.Asp406Asn
NM_000036.3:c.1129G>A MANE Select NP_000027.3:p.Asp377Asn
NM_001172626.2:c.1117G>A NP_001166097.2:p.Asp373Asn