Canonical Allele Identifier: CA2036910114

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53308772A= , CM000674.2:g.53308772A=	GRCh38
NC_000012.11:g.53702556A= , CM000674.1:g.53702556A=	GRCh37
NC_000012.10:g.51988823A=	NCBI36
NG_016775.1:g.17857T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1040T= MANE Select	ENSP00000209873.4:p.Val347=
ENST00000546562.6:n.2104T=
ENST00000547238.6:n.1676T=
ENST00000547520.6:n.1034T=
ENST00000547757.2:c.89T=	ENSP00000448020.2:p.Val30=
ENST00000548880.2:n.1490T=
ENST00000548931.6:c.560T=	ENSP00000457518.1:p.Val187=
ENST00000549450.6:n.974T=
ENST00000552161.6:n.1996T=
ENST00000672797.1:n.1529T=
ENST00000672900.1:n.1982T=
ENST00000209873.8:c.1040T=	ENSP00000209873.4:p.Val347=
ENST00000394384.7:c.941T=	ENSP00000377908.3:p.Val314=
ENST00000547520.5:n.744T=
ENST00000548931.5:c.560T=	ENSP00000457518.1:p.Val187=
ENST00000550033.5:n.295T=
ENST00000550286.5:c.668T=	ENSP00000446885.1:p.Val223=
ENST00000552876.5:n.1383T=
NM_001173466.1:c.941T=	NP_001166937.1:p.Val314=
NM_015665.5:c.1040T=	NP_056480.1:p.Val347=
XM_006719617.2:c.1055T=	XP_006719680.1:p.Val352=
XM_006719619.2:c.*50T=	XP_006719682.1:n.*50T=
XM_011538777.1:c.1055T=	XP_011537079.1:p.Val352=
XM_011538778.1:c.1040T=	XP_011537080.1:p.Val347=
XM_011538779.1:c.956T=	XP_011537081.1:p.Val319=
XM_011538780.1:c.941T=	XP_011537082.1:p.Val314=
XM_011538781.1:c.389T=	XP_011537083.1:p.Val130=
XM_011538778.2:c.1040T=	XP_011537080.1:p.Val347=
XM_011538780.2:c.941T=	XP_011537082.1:p.Val314=
XR_001748875.2:n.1097T=
NM_015665.6:c.1040T= MANE Select	NP_056480.1:p.Val347=
NM_001173466.2:c.941T=	NP_001166937.1:p.Val314=