Canonical Allele Identifier: CA2036909594

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307717C= , CM000674.2:g.53307717C=	GRCh38
NC_000012.11:g.53701501C= , CM000674.1:g.53701501C=	GRCh37
NC_000012.10:g.51987768C=	NCBI36
NG_016775.1:g.18912G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1417-4G= MANE Select	ENSP00000209873.4:n.1417-4G=
ENST00000546562.6:n.2481-4G=
ENST00000547238.6:n.2053-4G=
ENST00000547520.6:n.1533-4G=
ENST00000547757.2:c.*331G=	ENSP00000448020.2:n.*331G=
ENST00000548880.2:n.1867-4G=
ENST00000548931.6:c.852-4G=	ENSP00000457518.1:n.852-4G=
ENST00000549450.6:n.1351-4G=
ENST00000552161.6:n.2495-4G=
ENST00000672797.1:n.1906-4G=
ENST00000209873.8:c.1417-4G=	ENSP00000209873.4:n.1417-4G=
ENST00000394384.7:c.1318-4G=	ENSP00000377908.3:n.1318-4G=
ENST00000548931.5:c.852-4G=	ENSP00000457518.1:n.852-4G=
ENST00000550286.5:c.1045-4G=	ENSP00000446885.1:n.1045-4G=
ENST00000552876.5:n.1760-4G=
NM_001173466.1:c.1318-4G=	NP_001166937.1:n.1318-4G=
NM_015665.5:c.1417-4G=	NP_056480.1:n.1417-4G=
XM_006719617.2:c.1432-4G=	XP_006719680.1:n.1432-4G=
XM_011538777.1:c.1474-4G=	XP_011537079.1:n.1474-4G=
XM_011538778.1:c.1459-4G=	XP_011537080.1:n.1459-4G=
XM_011538779.1:c.1375-4G=	XP_011537081.1:n.1375-4G=
XM_011538780.1:c.1360-4G=	XP_011537082.1:n.1360-4G=
XM_011538781.1:c.808-4G=	XP_011537083.1:n.808-4G=
XM_011538778.2:c.1459-4G=	XP_011537080.1:n.1459-4G=
XM_011538780.2:c.1360-4G=	XP_011537082.1:n.1360-4G=
XR_001748875.2:n.1474-4G=
NM_015665.6:c.1417-4G= MANE Select	NP_056480.1:n.1417-4G=
NM_001173466.2:c.1318-4G=	NP_001166937.1:n.1318-4G=