Canonical Allele Identifier: CA385035063

Gene: AAAS

Linked Data

• COSMIC: COSM4043057
• MyVariant Identifiers: chr12:g.53701365G>T (hg19) ; chr12:g.53307581G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307581G>T , CM000674.2:g.53307581G>T	GRCh38
NC_000012.11:g.53701365G>T , CM000674.1:g.53701365G>T	GRCh37
NC_000012.10:g.51987632G>T	NCBI36
NG_016775.1:g.19048C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1549C>A MANE Select	ENSP00000209873.4:p.Leu517Ile
ENST00000546562.6:n.2613C>A
ENST00000547238.6:n.2185C>A
ENST00000547520.6:n.1665C>A
ENST00000547757.2:c.*467C>A	ENSP00000448020.2:n.*467C>A
ENST00000548931.6:c.984C>A	ENSP00000457518.1:p.Pro328=
ENST00000549450.6:n.1483C>A
ENST00000672797.1:n.2038C>A
ENST00000209873.8:c.1549C>A	ENSP00000209873.4:p.Leu517Ile
ENST00000394384.7:c.1450C>A	ENSP00000377908.3:p.Leu484Ile
ENST00000548931.5:c.984C>A	ENSP00000457518.1:p.Pro328=
ENST00000550286.5:c.1177C>A	ENSP00000446885.1:p.Leu393Ile
ENST00000552876.5:n.1892C>A
NM_001173466.1:c.1450C>A	NP_001166937.1:p.Leu484Ile
NM_015665.5:c.1549C>A	NP_056480.1:p.Leu517Ile
XM_006719617.2:c.1564C>A	XP_006719680.1:p.Leu522Ile
XM_011538777.1:c.1606C>A	XP_011537079.1:p.Leu536Ile
XM_011538778.1:c.1591C>A	XP_011537080.1:p.Leu531Ile
XM_011538779.1:c.1507C>A	XP_011537081.1:p.Leu503Ile
XM_011538780.1:c.1492C>A	XP_011537082.1:p.Leu498Ile
XM_011538781.1:c.940C>A	XP_011537083.1:p.Leu314Ile
XM_011538778.2:c.1591C>A	XP_011537080.1:p.Leu531Ile
XM_011538780.2:c.1492C>A	XP_011537082.1:p.Leu498Ile
XR_001748875.2:n.1606C>A
NM_015665.6:c.1549C>A MANE Select	NP_056480.1:p.Leu517Ile
NM_001173466.2:c.1450C>A	NP_001166937.1:p.Leu484Ile