Canonical Allele Identifier: CA385034982

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701354C>G (hg19) ; chr12:g.53307570C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307570C>G , CM000674.2:g.53307570C>G	GRCh38
NC_000012.11:g.53701354C>G , CM000674.1:g.53701354C>G	GRCh37
NC_000012.10:g.51987621C>G	NCBI36
NG_016775.1:g.19059G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1560G>C MANE Select	ENSP00000209873.4:p.Glu520Asp
ENST00000546562.6:n.2624G>C
ENST00000547238.6:n.2196G>C
ENST00000547520.6:n.1676G>C
ENST00000547757.2:c.*478G>C	ENSP00000448020.2:n.*478G>C
ENST00000548931.6:c.995G>C	ENSP00000457518.1:p.Arg332Thr
ENST00000549450.6:n.1494G>C
ENST00000672797.1:n.2049G>C
ENST00000209873.8:c.1560G>C	ENSP00000209873.4:p.Glu520Asp
ENST00000394384.7:c.1461G>C	ENSP00000377908.3:p.Glu487Asp
ENST00000548931.5:c.995G>C	ENSP00000457518.1:p.Arg332Thr
ENST00000550286.5:c.1188G>C	ENSP00000446885.1:p.Glu396Asp
ENST00000552876.5:n.1903G>C
NM_001173466.1:c.1461G>C	NP_001166937.1:p.Glu487Asp
NM_015665.5:c.1560G>C	NP_056480.1:p.Glu520Asp
XM_006719617.2:c.1575G>C	XP_006719680.1:p.Glu525Asp
XM_011538777.1:c.1617G>C	XP_011537079.1:p.Glu539Asp
XM_011538778.1:c.1602G>C	XP_011537080.1:p.Glu534Asp
XM_011538779.1:c.1518G>C	XP_011537081.1:p.Glu506Asp
XM_011538780.1:c.1503G>C	XP_011537082.1:p.Glu501Asp
XM_011538781.1:c.951G>C	XP_011537083.1:p.Glu317Asp
XM_011538778.2:c.1602G>C	XP_011537080.1:p.Glu534Asp
XM_011538780.2:c.1503G>C	XP_011537082.1:p.Glu501Asp
XR_001748875.2:n.1617G>C
NM_015665.6:c.1560G>C MANE Select	NP_056480.1:p.Glu520Asp
NM_001173466.2:c.1461G>C	NP_001166937.1:p.Glu487Asp