Canonical Allele Identifier: CA2036897481

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307461G= , CM000674.2:g.53307461G=	GRCh38
NC_000012.11:g.53701245G= , CM000674.1:g.53701245G=	GRCh37
NC_000012.10:g.51987512G=	NCBI36
NG_016775.1:g.19168C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.*28C= MANE Select	ENSP00000209873.4:n.*28C=
ENST00000548931.6:c.1104C=	ENSP00000457518.1:n.1104C=
ENST00000549450.6:n.1603C=
ENST00000209873.8:c.*28C=	ENSP00000209873.4:n.*28C=
ENST00000394384.7:c.*28C=	ENSP00000377908.3:n.*28C=
ENST00000550286.5:c.*28C=	ENSP00000446885.1:n.*28C=
ENST00000552876.5:n.2012C=
NM_001173466.1:c.*28C=	NP_001166937.1:n.*28C=
NM_015665.5:c.*28C=	NP_056480.1:n.*28C=
XM_006719617.2:c.*28C=	XP_006719680.1:n.*28C=
XM_011538777.1:c.*28C=	XP_011537079.1:n.*28C=
XM_011538778.1:c.*28C=	XP_011537080.1:n.*28C=
XM_011538779.1:c.*28C=	XP_011537081.1:n.*28C=
XM_011538780.1:c.*28C=	XP_011537082.1:n.*28C=
XM_011538781.1:c.*28C=	XP_011537083.1:n.*28C=
XM_011538778.2:c.*28C=	XP_011537080.1:n.*28C=
XM_011538780.2:c.*28C=	XP_011537082.1:n.*28C=
NM_015665.6:c.*28C= MANE Select	NP_056480.1:n.*28C=
NM_001173466.2:c.*28C=	NP_001166937.1:n.*28C=