Canonical Allele Identifier: CA2036909532

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307601C= , CM000674.2:g.53307601C=	GRCh38
NC_000012.11:g.53701385C= , CM000674.1:g.53701385C=	GRCh37
NC_000012.10:g.51987652C=	NCBI36
NG_016775.1:g.19028G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1529G= MANE Select	ENSP00000209873.4:p.Gly510=
ENST00000546562.6:n.2593G=
ENST00000547238.6:n.2165G=
ENST00000547520.6:n.1645G=
ENST00000547757.2:c.*447G=	ENSP00000448020.2:n.*447G=
ENST00000548931.6:c.964G=	ENSP00000457518.1:p.Ala322=
ENST00000549450.6:n.1463G=
ENST00000672797.1:n.2018G=
ENST00000209873.8:c.1529G=	ENSP00000209873.4:p.Gly510=
ENST00000394384.7:c.1430G=	ENSP00000377908.3:p.Gly477=
ENST00000548931.5:c.964G=	ENSP00000457518.1:p.Ala322=
ENST00000550286.5:c.1157G=	ENSP00000446885.1:p.Gly386=
ENST00000552876.5:n.1872G=
NM_001173466.1:c.1430G=	NP_001166937.1:p.Gly477=
NM_015665.5:c.1529G=	NP_056480.1:p.Gly510=
XM_006719617.2:c.1544G=	XP_006719680.1:p.Gly515=
XM_011538777.1:c.1586G=	XP_011537079.1:p.Gly529=
XM_011538778.1:c.1571G=	XP_011537080.1:p.Gly524=
XM_011538779.1:c.1487G=	XP_011537081.1:p.Gly496=
XM_011538780.1:c.1472G=	XP_011537082.1:p.Gly491=
XM_011538781.1:c.920G=	XP_011537083.1:p.Gly307=
XM_011538778.2:c.1571G=	XP_011537080.1:p.Gly524=
XM_011538780.2:c.1472G=	XP_011537082.1:p.Gly491=
XR_001748875.2:n.1586G=
NM_015665.6:c.1529G= MANE Select	NP_056480.1:p.Gly510=
NM_001173466.2:c.1430G=	NP_001166937.1:p.Gly477=