Canonical Allele Identifier: CA385034860

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701339A>G (hg19) ; chr12:g.53307555A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307555A>G , CM000674.2:g.53307555A>G	GRCh38
NC_000012.11:g.53701339A>G , CM000674.1:g.53701339A>G	GRCh37
NC_000012.10:g.51987606A>G	NCBI36
NG_016775.1:g.19074T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1575T>C MANE Select	ENSP00000209873.4:p.Ser525=
ENST00000546562.6:n.2639T>C
ENST00000547238.6:n.2211T>C
ENST00000547520.6:n.1691T>C
ENST00000547757.2:c.*493T>C	ENSP00000448020.2:n.*493T>C
ENST00000548931.6:c.1010T>C	ENSP00000457518.1:p.Leu337Pro
ENST00000549450.6:n.1509T>C
ENST00000672797.1:n.2064T>C
ENST00000209873.8:c.1575T>C	ENSP00000209873.4:p.Ser525=
ENST00000394384.7:c.1476T>C	ENSP00000377908.3:p.Ser492=
ENST00000548931.5:c.1010T>C	ENSP00000457518.1:p.Leu337Pro
ENST00000550286.5:c.1203T>C	ENSP00000446885.1:p.Ser401=
ENST00000552876.5:n.1918T>C
NM_001173466.1:c.1476T>C	NP_001166937.1:p.Ser492=
NM_015665.5:c.1575T>C	NP_056480.1:p.Ser525=
XM_006719617.2:c.1590T>C	XP_006719680.1:p.Ser530=
XM_011538777.1:c.1632T>C	XP_011537079.1:p.Ser544=
XM_011538778.1:c.1617T>C	XP_011537080.1:p.Ser539=
XM_011538779.1:c.1533T>C	XP_011537081.1:p.Ser511=
XM_011538780.1:c.1518T>C	XP_011537082.1:p.Ser506=
XM_011538781.1:c.966T>C	XP_011537083.1:p.Ser322=
XM_011538778.2:c.1617T>C	XP_011537080.1:p.Ser539=
XM_011538780.2:c.1518T>C	XP_011537082.1:p.Ser506=
XR_001748875.2:n.1632T>C
NM_015665.6:c.1575T>C MANE Select	NP_056480.1:p.Ser525=
NM_001173466.2:c.1476T>C	NP_001166937.1:p.Ser492=