Canonical Allele Identifier: CA385040558

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53702560T>A (hg19) ; chr12:g.53308776T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53308776T>A , CM000674.2:g.53308776T>A	GRCh38
NC_000012.11:g.53702560T>A , CM000674.1:g.53702560T>A	GRCh37
NC_000012.10:g.51988827T>A	NCBI36
NG_016775.1:g.17853A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1036A>T MANE Select	ENSP00000209873.4:p.Thr346Ser
ENST00000546393.7:n.1881A>T
ENST00000546562.6:n.2100A>T
ENST00000547238.6:n.1672A>T
ENST00000547520.6:n.1030A>T
ENST00000547757.2:c.85A>T	ENSP00000448020.2:p.Thr29Ser
ENST00000548880.2:n.1486A>T
ENST00000548931.6:c.556A>T	ENSP00000457518.1:p.Thr186Ser
ENST00000549450.6:n.970A>T
ENST00000552161.6:n.1992A>T
ENST00000672797.1:n.1525A>T
ENST00000672900.1:n.1978A>T
ENST00000209873.8:c.1036A>T	ENSP00000209873.4:p.Thr346Ser
ENST00000394384.7:c.937A>T	ENSP00000377908.3:p.Thr313Ser
ENST00000547520.5:n.740A>T
ENST00000548931.5:c.556A>T	ENSP00000457518.1:p.Thr186Ser
ENST00000550033.5:n.291A>T
ENST00000550286.5:c.664A>T	ENSP00000446885.1:p.Thr222Ser
ENST00000552876.5:n.1379A>T
NM_001173466.1:c.937A>T	NP_001166937.1:p.Thr313Ser
NM_015665.5:c.1036A>T	NP_056480.1:p.Thr346Ser
XM_006719617.2:c.1051A>T	XP_006719680.1:p.Thr351Ser
XM_006719619.2:c.*46A>T	XP_006719682.1:n.*46A>T
XM_011538777.1:c.1051A>T	XP_011537079.1:p.Thr351Ser
XM_011538778.1:c.1036A>T	XP_011537080.1:p.Thr346Ser
XM_011538779.1:c.952A>T	XP_011537081.1:p.Thr318Ser
XM_011538780.1:c.937A>T	XP_011537082.1:p.Thr313Ser
XM_011538781.1:c.385A>T	XP_011537083.1:p.Thr129Ser
XM_011538778.2:c.1036A>T	XP_011537080.1:p.Thr346Ser
XM_011538780.2:c.937A>T	XP_011537082.1:p.Thr313Ser
XR_001748875.2:n.1093A>T
NM_015665.6:c.1036A>T MANE Select	NP_056480.1:p.Thr346Ser
NM_001173466.2:c.937A>T	NP_001166937.1:p.Thr313Ser