Canonical Allele Identifier: CA2036909492

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307513G= , CM000674.2:g.53307513G=	GRCh38
NC_000012.11:g.53701297G= , CM000674.1:g.53701297G=	GRCh37
NC_000012.10:g.51987564G=	NCBI36
NG_016775.1:g.19116C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1617C= MANE Select	ENSP00000209873.4:p.Pro539=
ENST00000546562.6:n.2681C=
ENST00000547757.2:c.*535C=	ENSP00000448020.2:n.*535C=
ENST00000548931.6:c.1052C=	ENSP00000457518.1:p.Pro351=
ENST00000549450.6:n.1551C=
ENST00000209873.8:c.1617C=	ENSP00000209873.4:p.Pro539=
ENST00000394384.7:c.1518C=	ENSP00000377908.3:p.Pro506=
ENST00000548931.5:c.1052C=	ENSP00000457518.1:p.Pro351=
ENST00000550286.5:c.1245C=	ENSP00000446885.1:p.Pro415=
ENST00000552876.5:n.1960C=
NM_001173466.1:c.1518C=	NP_001166937.1:p.Pro506=
NM_015665.5:c.1617C=	NP_056480.1:p.Pro539=
XM_006719617.2:c.1632C=	XP_006719680.1:p.Pro544=
XM_011538777.1:c.1674C=	XP_011537079.1:p.Pro558=
XM_011538778.1:c.1659C=	XP_011537080.1:p.Pro553=
XM_011538779.1:c.1575C=	XP_011537081.1:p.Pro525=
XM_011538780.1:c.1560C=	XP_011537082.1:p.Pro520=
XM_011538781.1:c.1008C=	XP_011537083.1:p.Pro336=
XM_011538778.2:c.1659C=	XP_011537080.1:p.Pro553=
XM_011538780.2:c.1560C=	XP_011537082.1:p.Pro520=
XR_001748875.2:n.1674C=
NM_015665.6:c.1617C= MANE Select	NP_056480.1:p.Pro539=
NM_001173466.2:c.1518C=	NP_001166937.1:p.Pro506=