Canonical Allele Identifier: CA2036910228

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53309002C= , CM000674.2:g.53309002C=	GRCh38
NC_000012.11:g.53702786C= , CM000674.1:g.53702786C=	GRCh37
NC_000012.10:g.51989053C=	NCBI36
NG_016775.1:g.17627G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.954G= MANE Select	ENSP00000209873.4:p.Met318=
ENST00000546393.7:n.1799G=
ENST00000546562.6:n.2018G=
ENST00000547238.6:n.1590G=
ENST00000547520.6:n.948G=
ENST00000547757.2:c.3G=	ENSP00000448020.2:p.Met1=
ENST00000548880.2:n.1404G=
ENST00000548931.6:c.474G=	ENSP00000457518.1:p.Met158=
ENST00000549450.6:n.888G=
ENST00000552161.6:n.1910G=
ENST00000672797.1:n.1407G=
ENST00000672900.1:n.1752G=
ENST00000209873.8:c.954G=	ENSP00000209873.4:p.Met318=
ENST00000394384.7:c.855G=	ENSP00000377908.3:p.Met285=
ENST00000546572.1:n.542G=
ENST00000547520.5:n.658G=
ENST00000548931.5:c.474G=	ENSP00000457518.1:p.Met158=
ENST00000550033.5:n.209G=
ENST00000550286.5:c.582G=	ENSP00000446885.1:p.Met194=
ENST00000552876.5:n.1297G=
NM_001173466.1:c.855G=	NP_001166937.1:p.Met285=
NM_015665.5:c.954G=	NP_056480.1:p.Met318=
XM_006719617.2:c.969G=	XP_006719680.1:p.Met323=
XM_006719619.2:c.969G=	XP_006719682.1:p.Met323=
XM_011538777.1:c.969G=	XP_011537079.1:p.Met323=
XM_011538778.1:c.954G=	XP_011537080.1:p.Met318=
XM_011538779.1:c.870G=	XP_011537081.1:p.Met290=
XM_011538780.1:c.855G=	XP_011537082.1:p.Met285=
XM_011538781.1:c.303G=	XP_011537083.1:p.Met101=
XM_011538778.2:c.954G=	XP_011537080.1:p.Met318=
XM_011538780.2:c.855G=	XP_011537082.1:p.Met285=
XR_001748875.2:n.975G=
NM_015665.6:c.954G= MANE Select	NP_056480.1:p.Met318=
NM_001173466.2:c.855G=	NP_001166937.1:p.Met285=