Canonical Allele Identifier: CA385035344

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701409T>A (hg19) ; chr12:g.53307625T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307625T>A , CM000674.2:g.53307625T>A	GRCh38
NC_000012.11:g.53701409T>A , CM000674.1:g.53701409T>A	GRCh37
NC_000012.10:g.51987676T>A	NCBI36
NG_016775.1:g.19004A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1505A>T MANE Select	ENSP00000209873.4:p.Gln502Leu
ENST00000546562.6:n.2569A>T
ENST00000547238.6:n.2141A>T
ENST00000547520.6:n.1621A>T
ENST00000547757.2:c.*423A>T	ENSP00000448020.2:n.*423A>T
ENST00000548931.6:c.940A>T	ENSP00000457518.1:p.Arg314Trp
ENST00000549450.6:n.1439A>T
ENST00000672797.1:n.1994A>T
ENST00000209873.8:c.1505A>T	ENSP00000209873.4:p.Gln502Leu
ENST00000394384.7:c.1406A>T	ENSP00000377908.3:p.Gln469Leu
ENST00000548931.5:c.940A>T	ENSP00000457518.1:p.Arg314Trp
ENST00000550286.5:c.1133A>T	ENSP00000446885.1:p.Gln378Leu
ENST00000552876.5:n.1848A>T
NM_001173466.1:c.1406A>T	NP_001166937.1:p.Gln469Leu
NM_015665.5:c.1505A>T	NP_056480.1:p.Gln502Leu
XM_006719617.2:c.1520A>T	XP_006719680.1:p.Gln507Leu
XM_011538777.1:c.1562A>T	XP_011537079.1:p.Gln521Leu
XM_011538778.1:c.1547A>T	XP_011537080.1:p.Gln516Leu
XM_011538779.1:c.1463A>T	XP_011537081.1:p.Gln488Leu
XM_011538780.1:c.1448A>T	XP_011537082.1:p.Gln483Leu
XM_011538781.1:c.896A>T	XP_011537083.1:p.Gln299Leu
XM_011538778.2:c.1547A>T	XP_011537080.1:p.Gln516Leu
XM_011538780.2:c.1448A>T	XP_011537082.1:p.Gln483Leu
XR_001748875.2:n.1562A>T
NM_015665.6:c.1505A>T MANE Select	NP_056480.1:p.Gln502Leu
NM_001173466.2:c.1406A>T	NP_001166937.1:p.Gln469Leu