Canonical Allele Identifier: CA341748971
Gene: AMPD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677924C>A , CM000663.2:g.114677924C>A GRCh38
NC_000001.10:g.115220545C>A , CM000663.1:g.115220545C>A GRCh37
NC_000001.9:g.115022068C>A NCBI36
NG_008012.1:g.22632G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1198G>T ENSP00000358551.4:p.Ala400Ser
ENST00000520113.7:c.1210G>T MANE Select ENSP00000430075.3:p.Ala404Ser
ENST00000637080.1:c.993G>T ENSP00000489753.1:n.993G>T
ENST00000639077.1:n.875G>T
ENST00000369538.3:c.1297G>T ENSP00000358551.3:p.Ala433Ser
ENST00000520113.6:c.1309G>T ENSP00000430075.2:p.Ala437Ser
NM_000036.2:c.1309G>T NP_000027.2:p.Ala437Ser
NM_001172626.1:c.1297G>T NP_001166097.1:p.Ala433Ser
NM_000036.3:c.1210G>T MANE Select NP_000027.3:p.Ala404Ser
NM_001172626.2:c.1198G>T NP_001166097.2:p.Ala400Ser