Canonical Allele Identifier: CA2036910140

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53308826G= , CM000674.2:g.53308826G=	GRCh38
NC_000012.11:g.53702610G= , CM000674.1:g.53702610G=	GRCh37
NC_000012.10:g.51988877G=	NCBI36
NG_016775.1:g.17803C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.997-11C= MANE Select	ENSP00000209873.4:n.997-11C=
ENST00000546393.7:n.1842-11C=
ENST00000546562.6:n.2061-11C=
ENST00000547238.6:n.1633-11C=
ENST00000547520.6:n.991-11C=
ENST00000547757.2:c.46-11C=	ENSP00000448020.2:n.46-11C=
ENST00000548880.2:n.1447-11C=
ENST00000548931.6:c.517-11C=	ENSP00000457518.1:n.517-11C=
ENST00000549450.6:n.931-11C=
ENST00000552161.6:n.1953-11C=
ENST00000672797.1:n.1475C=
ENST00000672900.1:n.1928C=
ENST00000209873.8:c.997-11C=	ENSP00000209873.4:n.997-11C=
ENST00000394384.7:c.898-11C=	ENSP00000377908.3:n.898-11C=
ENST00000547520.5:n.701-11C=
ENST00000548931.5:c.517-11C=	ENSP00000457518.1:n.517-11C=
ENST00000550033.5:n.252-11C=
ENST00000550286.5:c.625-11C=	ENSP00000446885.1:n.625-11C=
ENST00000552876.5:n.1340-11C=
NM_001173466.1:c.898-11C=	NP_001166937.1:n.898-11C=
NM_015665.5:c.997-11C=	NP_056480.1:n.997-11C=
XM_006719617.2:c.1012-11C=	XP_006719680.1:n.1012-11C=
XM_006719619.2:c.1037C=	XP_006719682.1:p.Pro346=
XM_011538777.1:c.1012-11C=	XP_011537079.1:n.1012-11C=
XM_011538778.1:c.997-11C=	XP_011537080.1:n.997-11C=
XM_011538779.1:c.913-11C=	XP_011537081.1:n.913-11C=
XM_011538780.1:c.898-11C=	XP_011537082.1:n.898-11C=
XM_011538781.1:c.346-11C=	XP_011537083.1:n.346-11C=
XM_011538778.2:c.997-11C=	XP_011537080.1:n.997-11C=
XM_011538780.2:c.898-11C=	XP_011537082.1:n.898-11C=
XR_001748875.2:n.1043C=
NM_015665.6:c.997-11C= MANE Select	NP_056480.1:n.997-11C=
NM_001173466.2:c.898-11C=	NP_001166937.1:n.898-11C=