Canonical Allele Identifier: CA2036910128

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53308803T= , CM000674.2:g.53308803T=	GRCh38
NC_000012.11:g.53702587T= , CM000674.1:g.53702587T=	GRCh37
NC_000012.10:g.51988854T=	NCBI36
NG_016775.1:g.17826A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1009A= MANE Select	ENSP00000209873.4:p.Ser337=
ENST00000546393.7:n.1854A=
ENST00000546562.6:n.2073A=
ENST00000547238.6:n.1645A=
ENST00000547520.6:n.1003A=
ENST00000547757.2:c.58A=	ENSP00000448020.2:p.Ser20=
ENST00000548880.2:n.1459A=
ENST00000548931.6:c.529A=	ENSP00000457518.1:p.Ser177=
ENST00000549450.6:n.943A=
ENST00000552161.6:n.1965A=
ENST00000672797.1:n.1498A=
ENST00000672900.1:n.1951A=
ENST00000209873.8:c.1009A=	ENSP00000209873.4:p.Ser337=
ENST00000394384.7:c.910A=	ENSP00000377908.3:p.Ser304=
ENST00000547520.5:n.713A=
ENST00000548931.5:c.529A=	ENSP00000457518.1:p.Ser177=
ENST00000550033.5:n.264A=
ENST00000550286.5:c.637A=	ENSP00000446885.1:p.Ser213=
ENST00000552876.5:n.1352A=
NM_001173466.1:c.910A=	NP_001166937.1:p.Ser304=
NM_015665.5:c.1009A=	NP_056480.1:p.Ser337=
XM_006719617.2:c.1024A=	XP_006719680.1:p.Ser342=
XM_006719619.2:c.*19A=	XP_006719682.1:n.*19A=
XM_011538777.1:c.1024A=	XP_011537079.1:p.Ser342=
XM_011538778.1:c.1009A=	XP_011537080.1:p.Ser337=
XM_011538779.1:c.925A=	XP_011537081.1:p.Ser309=
XM_011538780.1:c.910A=	XP_011537082.1:p.Ser304=
XM_011538781.1:c.358A=	XP_011537083.1:p.Ser120=
XM_011538778.2:c.1009A=	XP_011537080.1:p.Ser337=
XM_011538780.2:c.910A=	XP_011537082.1:p.Ser304=
XR_001748875.2:n.1066A=
NM_015665.6:c.1009A= MANE Select	NP_056480.1:p.Ser337=
NM_001173466.2:c.910A=	NP_001166937.1:p.Ser304=