Canonical Allele Identifier: CA385034398
Gene: AAAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53307491A>T , CM000674.2:g.53307491A>T GRCh38
NC_000012.11:g.53701275A>T , CM000674.1:g.53701275A>T GRCh37
NC_000012.10:g.51987542A>T NCBI36
NG_016775.1:g.19138T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000209873.9:c.1639T>A MANE Select ENSP00000209873.4:p.Ter547Lys
ENST00000547757.2:c.*557T>A ENSP00000448020.2:n.*557T>A
ENST00000548931.6:c.1074T>A ENSP00000457518.1:p.Ser358=
ENST00000549450.6:n.1573T>A
ENST00000209873.8:c.1639T>A ENSP00000209873.4:p.Ter547Lys
ENST00000394384.7:c.1540T>A ENSP00000377908.3:p.Ter514Lys
ENST00000548931.5:c.1074T>A ENSP00000457518.1:p.Ser358=
ENST00000550286.5:c.1267T>A ENSP00000446885.1:p.Ter423Lys
ENST00000552876.5:n.1982T>A
NM_001173466.1:c.1540T>A NP_001166937.1:p.Ter514Lys
NM_015665.5:c.1639T>A NP_056480.1:p.Ter547Lys
XM_006719617.2:c.1654T>A XP_006719680.1:p.Ter552Lys
XM_011538777.1:c.1696T>A XP_011537079.1:p.Ter566Lys
XM_011538778.1:c.1681T>A XP_011537080.1:p.Ter561Lys
XM_011538779.1:c.1597T>A XP_011537081.1:p.Ter533Lys
XM_011538780.1:c.1582T>A XP_011537082.1:p.Ter528Lys
XM_011538781.1:c.1030T>A XP_011537083.1:p.Ter344Lys
XM_011538778.2:c.1681T>A XP_011537080.1:p.Ter561Lys
XM_011538780.2:c.1582T>A XP_011537082.1:p.Ter528Lys
XR_001748875.2:n.1696T>A
NM_015665.6:c.1639T>A MANE Select NP_056480.1:p.Ter547Lys
NM_001173466.2:c.1540T>A NP_001166937.1:p.Ter514Lys