Canonical Allele Identifier: CA385037488

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701495G>C (hg19) ; chr12:g.53307711G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307711G>C , CM000674.2:g.53307711G>C	GRCh38
NC_000012.11:g.53701495G>C , CM000674.1:g.53701495G>C	GRCh37
NC_000012.10:g.51987762G>C	NCBI36
NG_016775.1:g.18918C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1419C>G MANE Select	ENSP00000209873.4:p.Gly473=
ENST00000546562.6:n.2483C>G
ENST00000547238.6:n.2055C>G
ENST00000547520.6:n.1535C>G
ENST00000547757.2:c.*337C>G	ENSP00000448020.2:n.*337C>G
ENST00000548880.2:n.1869C>G
ENST00000548931.6:c.854C>G	ENSP00000457518.1:p.Ala285Gly
ENST00000549450.6:n.1353C>G
ENST00000552161.6:n.2497C>G
ENST00000672797.1:n.1908C>G
ENST00000209873.8:c.1419C>G	ENSP00000209873.4:p.Gly473=
ENST00000394384.7:c.1320C>G	ENSP00000377908.3:p.Gly440=
ENST00000548931.5:c.854C>G	ENSP00000457518.1:p.Ala285Gly
ENST00000550286.5:c.1047C>G	ENSP00000446885.1:p.Gly349=
ENST00000552876.5:n.1762C>G
NM_001173466.1:c.1320C>G	NP_001166937.1:p.Gly440=
NM_015665.5:c.1419C>G	NP_056480.1:p.Gly473=
XM_006719617.2:c.1434C>G	XP_006719680.1:p.Gly478=
XM_011538777.1:c.1476C>G	XP_011537079.1:p.Gly492=
XM_011538778.1:c.1461C>G	XP_011537080.1:p.Gly487=
XM_011538779.1:c.1377C>G	XP_011537081.1:p.Gly459=
XM_011538780.1:c.1362C>G	XP_011537082.1:p.Gly454=
XM_011538781.1:c.810C>G	XP_011537083.1:p.Gly270=
XM_011538778.2:c.1461C>G	XP_011537080.1:p.Gly487=
XM_011538780.2:c.1362C>G	XP_011537082.1:p.Gly454=
XR_001748875.2:n.1476C>G
NM_015665.6:c.1419C>G MANE Select	NP_056480.1:p.Gly473=
NM_001173466.2:c.1320C>G	NP_001166937.1:p.Gly440=