Canonical Allele Identifier: CA385034450

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701282G>T (hg19) ; chr12:g.53307498G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307498G>T , CM000674.2:g.53307498G>T	GRCh38
NC_000012.11:g.53701282G>T , CM000674.1:g.53701282G>T	GRCh37
NC_000012.10:g.51987549G>T	NCBI36
NG_016775.1:g.19131C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1632C>A MANE Select	ENSP00000209873.4:p.Ser544=
ENST00000547757.2:c.*550C>A	ENSP00000448020.2:n.*550C>A
ENST00000548931.6:c.1067C>A	ENSP00000457518.1:p.Pro356His
ENST00000549450.6:n.1566C>A
ENST00000209873.8:c.1632C>A	ENSP00000209873.4:p.Ser544=
ENST00000394384.7:c.1533C>A	ENSP00000377908.3:p.Ser511=
ENST00000548931.5:c.1067C>A	ENSP00000457518.1:p.Pro356His
ENST00000550286.5:c.1260C>A	ENSP00000446885.1:p.Ser420=
ENST00000552876.5:n.1975C>A
NM_001173466.1:c.1533C>A	NP_001166937.1:p.Ser511=
NM_015665.5:c.1632C>A	NP_056480.1:p.Ser544=
XM_006719617.2:c.1647C>A	XP_006719680.1:p.Ser549=
XM_011538777.1:c.1689C>A	XP_011537079.1:p.Ser563=
XM_011538778.1:c.1674C>A	XP_011537080.1:p.Ser558=
XM_011538779.1:c.1590C>A	XP_011537081.1:p.Ser530=
XM_011538780.1:c.1575C>A	XP_011537082.1:p.Ser525=
XM_011538781.1:c.1023C>A	XP_011537083.1:p.Ser341=
XM_011538778.2:c.1674C>A	XP_011537080.1:p.Ser558=
XM_011538780.2:c.1575C>A	XP_011537082.1:p.Ser525=
XR_001748875.2:n.1689C>A
NM_015665.6:c.1632C>A MANE Select	NP_056480.1:p.Ser544=
NM_001173466.2:c.1533C>A	NP_001166937.1:p.Ser511=