Canonical Allele Identifier: CA2036910210
Gene: AAAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.53308964C= , CM000674.2:g.53308964C= GRCh38
NC_000012.11:g.53702748C= , CM000674.1:g.53702748C= GRCh37
NC_000012.10:g.51989015C= NCBI36
NG_016775.1:g.17665G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000209873.9:c.992G= MANE Select ENSP00000209873.4:p.Cys331=
ENST00000546393.7:n.1837G=
ENST00000546562.6:n.2056G=
ENST00000547238.6:n.1628G=
ENST00000547520.6:n.986G=
ENST00000547757.2:c.41G= ENSP00000448020.2:p.Cys14=
ENST00000548880.2:n.1442G=
ENST00000548931.6:c.512G= ENSP00000457518.1:p.Cys171=
ENST00000549450.6:n.926G=
ENST00000552161.6:n.1948G=
ENST00000672797.1:n.1445G=
ENST00000672900.1:n.1790G=
ENST00000209873.8:c.992G= ENSP00000209873.4:p.Cys331=
ENST00000394384.7:c.893G= ENSP00000377908.3:p.Cys298=
ENST00000546572.1:n.580G=
ENST00000547520.5:n.696G=
ENST00000548931.5:c.512G= ENSP00000457518.1:p.Cys171=
ENST00000550033.5:n.247G=
ENST00000550286.5:c.620G= ENSP00000446885.1:p.Cys207=
ENST00000552876.5:n.1335G=
NM_001173466.1:c.893G= NP_001166937.1:p.Cys298=
NM_015665.5:c.992G= NP_056480.1:p.Cys331=
XM_006719617.2:c.1007G= XP_006719680.1:p.Cys336=
XM_006719619.2:c.1007G= XP_006719682.1:p.Cys336=
XM_011538777.1:c.1007G= XP_011537079.1:p.Cys336=
XM_011538778.1:c.992G= XP_011537080.1:p.Cys331=
XM_011538779.1:c.908G= XP_011537081.1:p.Cys303=
XM_011538780.1:c.893G= XP_011537082.1:p.Cys298=
XM_011538781.1:c.341G= XP_011537083.1:p.Cys114=
XM_011538778.2:c.992G= XP_011537080.1:p.Cys331=
XM_011538780.2:c.893G= XP_011537082.1:p.Cys298=
XR_001748875.2:n.1013G=
NM_015665.6:c.992G= MANE Select NP_056480.1:p.Cys331=
NM_001173466.2:c.893G= NP_001166937.1:p.Cys298=