Canonical Allele Identifier: CA2036909576

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307678C= , CM000674.2:g.53307678C=	GRCh38
NC_000012.11:g.53701462C= , CM000674.1:g.53701462C=	GRCh37
NC_000012.10:g.51987729C=	NCBI36
NG_016775.1:g.18951G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1452G= MANE Select	ENSP00000209873.4:p.Leu484=
ENST00000546562.6:n.2516G=
ENST00000547238.6:n.2088G=
ENST00000547520.6:n.1568G=
ENST00000547757.2:c.*370G=	ENSP00000448020.2:n.*370G=
ENST00000548880.2:n.1902G=
ENST00000548931.6:c.887G=	ENSP00000457518.1:p.Cys296=
ENST00000549450.6:n.1386G=
ENST00000552161.6:n.2530G=
ENST00000672797.1:n.1941G=
ENST00000209873.8:c.1452G=	ENSP00000209873.4:p.Leu484=
ENST00000394384.7:c.1353G=	ENSP00000377908.3:p.Leu451=
ENST00000548931.5:c.887G=	ENSP00000457518.1:p.Cys296=
ENST00000550286.5:c.1080G=	ENSP00000446885.1:p.Leu360=
ENST00000552876.5:n.1795G=
NM_001173466.1:c.1353G=	NP_001166937.1:p.Leu451=
NM_015665.5:c.1452G=	NP_056480.1:p.Leu484=
XM_006719617.2:c.1467G=	XP_006719680.1:p.Leu489=
XM_011538777.1:c.1509G=	XP_011537079.1:p.Leu503=
XM_011538778.1:c.1494G=	XP_011537080.1:p.Leu498=
XM_011538779.1:c.1410G=	XP_011537081.1:p.Leu470=
XM_011538780.1:c.1395G=	XP_011537082.1:p.Leu465=
XM_011538781.1:c.843G=	XP_011537083.1:p.Leu281=
XM_011538778.2:c.1494G=	XP_011537080.1:p.Leu498=
XM_011538780.2:c.1395G=	XP_011537082.1:p.Leu465=
XR_001748875.2:n.1509G=
NM_015665.6:c.1452G= MANE Select	NP_056480.1:p.Leu484=
NM_001173466.2:c.1353G=	NP_001166937.1:p.Leu451=