Canonical Allele Identifier: CA2036910308
Gene: AAAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53309169G= , CM000674.2:g.53309169G= GRCh38
NC_000012.11:g.53702953G= , CM000674.1:g.53702953G= GRCh37
NC_000012.10:g.51989220G= NCBI36
NG_016775.1:g.17460C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000209873.9:c.923C= MANE Select ENSP00000209873.4:p.Ser308=
ENST00000546393.7:n.1768C=
ENST00000546562.6:n.1987C=
ENST00000547238.6:n.1559C=
ENST00000547520.6:n.917C=
ENST00000547757.2:c.-29C= ENSP00000448020.2:n.-29C=
ENST00000548880.2:n.1373C=
ENST00000548931.6:c.443C= ENSP00000457518.1:p.Ser148=
ENST00000549450.6:n.857C=
ENST00000552161.6:n.1879C=
ENST00000672797.1:n.1376C=
ENST00000672900.1:n.1721C=
ENST00000209873.8:c.923C= ENSP00000209873.4:p.Ser308=
ENST00000394384.7:c.824C= ENSP00000377908.3:p.Ser275=
ENST00000546393.6:n.820C=
ENST00000546572.1:n.375C=
ENST00000547520.5:n.627C=
ENST00000547757.1:c.824C= ENSP00000448020.1:p.Ser275=
ENST00000547761.6:n.815C=
ENST00000548931.5:c.443C= ENSP00000457518.1:p.Ser148=
ENST00000550033.5:n.178C=
ENST00000550286.5:c.551C= ENSP00000446885.1:p.Ser184=
ENST00000552876.5:n.1266C=
NM_001173466.1:c.824C= NP_001166937.1:p.Ser275=
NM_015665.5:c.923C= NP_056480.1:p.Ser308=
XM_006719617.2:c.938C= XP_006719680.1:p.Ser313=
XM_006719619.2:c.938C= XP_006719682.1:p.Ser313=
XM_011538777.1:c.938C= XP_011537079.1:p.Ser313=
XM_011538778.1:c.923C= XP_011537080.1:p.Ser308=
XM_011538779.1:c.839C= XP_011537081.1:p.Ser280=
XM_011538780.1:c.824C= XP_011537082.1:p.Ser275=
XM_011538781.1:c.272C= XP_011537083.1:p.Ser91=
XM_011538778.2:c.923C= XP_011537080.1:p.Ser308=
XM_011538780.2:c.824C= XP_011537082.1:p.Ser275=
XR_001748875.2:n.944C=
NM_015665.6:c.923C= MANE Select NP_056480.1:p.Ser308=
NM_001173466.2:c.824C= NP_001166937.1:p.Ser275=