Canonical Allele Identifier: CA385035278

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701397G>T (hg19) ; chr12:g.53307613G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307613G>T , CM000674.2:g.53307613G>T	GRCh38
NC_000012.11:g.53701397G>T , CM000674.1:g.53701397G>T	GRCh37
NC_000012.10:g.51987664G>T	NCBI36
NG_016775.1:g.19016C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1517C>A MANE Select	ENSP00000209873.4:p.Ala506Asp
ENST00000546562.6:n.2581C>A
ENST00000547238.6:n.2153C>A
ENST00000547520.6:n.1633C>A
ENST00000547757.2:c.*435C>A	ENSP00000448020.2:n.*435C>A
ENST00000548931.6:c.952C>A	ENSP00000457518.1:p.Leu318Met
ENST00000549450.6:n.1451C>A
ENST00000672797.1:n.2006C>A
ENST00000209873.8:c.1517C>A	ENSP00000209873.4:p.Ala506Asp
ENST00000394384.7:c.1418C>A	ENSP00000377908.3:p.Ala473Asp
ENST00000548931.5:c.952C>A	ENSP00000457518.1:p.Leu318Met
ENST00000550286.5:c.1145C>A	ENSP00000446885.1:p.Ala382Asp
ENST00000552876.5:n.1860C>A
NM_001173466.1:c.1418C>A	NP_001166937.1:p.Ala473Asp
NM_015665.5:c.1517C>A	NP_056480.1:p.Ala506Asp
XM_006719617.2:c.1532C>A	XP_006719680.1:p.Ala511Asp
XM_011538777.1:c.1574C>A	XP_011537079.1:p.Ala525Asp
XM_011538778.1:c.1559C>A	XP_011537080.1:p.Ala520Asp
XM_011538779.1:c.1475C>A	XP_011537081.1:p.Ala492Asp
XM_011538780.1:c.1460C>A	XP_011537082.1:p.Ala487Asp
XM_011538781.1:c.908C>A	XP_011537083.1:p.Ala303Asp
XM_011538778.2:c.1559C>A	XP_011537080.1:p.Ala520Asp
XM_011538780.2:c.1460C>A	XP_011537082.1:p.Ala487Asp
XR_001748875.2:n.1574C>A
NM_015665.6:c.1517C>A MANE Select	NP_056480.1:p.Ala506Asp
NM_001173466.2:c.1418C>A	NP_001166937.1:p.Ala473Asp