Canonical Allele Identifier: CA385041142

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53702764T>A (hg19) ; chr12:g.53308980T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53308980T>A , CM000674.2:g.53308980T>A	GRCh38
NC_000012.11:g.53702764T>A , CM000674.1:g.53702764T>A	GRCh37
NC_000012.10:g.51989031T>A	NCBI36
NG_016775.1:g.17649A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.976A>T MANE Select	ENSP00000209873.4:p.Thr326Ser
ENST00000546393.7:n.1821A>T
ENST00000546562.6:n.2040A>T
ENST00000547238.6:n.1612A>T
ENST00000547520.6:n.970A>T
ENST00000547757.2:c.25A>T	ENSP00000448020.2:p.Thr9Ser
ENST00000548880.2:n.1426A>T
ENST00000548931.6:c.496A>T	ENSP00000457518.1:p.Thr166Ser
ENST00000549450.6:n.910A>T
ENST00000552161.6:n.1932A>T
ENST00000672797.1:n.1429A>T
ENST00000672900.1:n.1774A>T
ENST00000209873.8:c.976A>T	ENSP00000209873.4:p.Thr326Ser
ENST00000394384.7:c.877A>T	ENSP00000377908.3:p.Thr293Ser
ENST00000546572.1:n.564A>T
ENST00000547520.5:n.680A>T
ENST00000548931.5:c.496A>T	ENSP00000457518.1:p.Thr166Ser
ENST00000550033.5:n.231A>T
ENST00000550286.5:c.604A>T	ENSP00000446885.1:p.Thr202Ser
ENST00000552876.5:n.1319A>T
NM_001173466.1:c.877A>T	NP_001166937.1:p.Thr293Ser
NM_015665.5:c.976A>T	NP_056480.1:p.Thr326Ser
XM_006719617.2:c.991A>T	XP_006719680.1:p.Thr331Ser
XM_006719619.2:c.991A>T	XP_006719682.1:p.Thr331Ser
XM_011538777.1:c.991A>T	XP_011537079.1:p.Thr331Ser
XM_011538778.1:c.976A>T	XP_011537080.1:p.Thr326Ser
XM_011538779.1:c.892A>T	XP_011537081.1:p.Thr298Ser
XM_011538780.1:c.877A>T	XP_011537082.1:p.Thr293Ser
XM_011538781.1:c.325A>T	XP_011537083.1:p.Thr109Ser
XM_011538778.2:c.976A>T	XP_011537080.1:p.Thr326Ser
XM_011538780.2:c.877A>T	XP_011537082.1:p.Thr293Ser
XR_001748875.2:n.997A>T
NM_015665.6:c.976A>T MANE Select	NP_056480.1:p.Thr326Ser
NM_001173466.2:c.877A>T	NP_001166937.1:p.Thr293Ser