Canonical Allele Identifier: CA2036909488

Gene: AAAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307506G= , CM000674.2:g.53307506G=	GRCh38
NC_000012.11:g.53701290G= , CM000674.1:g.53701290G=	GRCh37
NC_000012.10:g.51987557G=	NCBI36
NG_016775.1:g.19123C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1624C= MANE Select	ENSP00000209873.4:p.Pro542=
ENST00000546562.6:n.2688C=
ENST00000547757.2:c.*542C=	ENSP00000448020.2:n.*542C=
ENST00000548931.6:c.1059C=	ENSP00000457518.1:p.Pro353=
ENST00000549450.6:n.1558C=
ENST00000209873.8:c.1624C=	ENSP00000209873.4:p.Pro542=
ENST00000394384.7:c.1525C=	ENSP00000377908.3:p.Pro509=
ENST00000548931.5:c.1059C=	ENSP00000457518.1:p.Pro353=
ENST00000550286.5:c.1252C=	ENSP00000446885.1:p.Pro418=
ENST00000552876.5:n.1967C=
NM_001173466.1:c.1525C=	NP_001166937.1:p.Pro509=
NM_015665.5:c.1624C=	NP_056480.1:p.Pro542=
XM_006719617.2:c.1639C=	XP_006719680.1:p.Pro547=
XM_011538777.1:c.1681C=	XP_011537079.1:p.Pro561=
XM_011538778.1:c.1666C=	XP_011537080.1:p.Pro556=
XM_011538779.1:c.1582C=	XP_011537081.1:p.Pro528=
XM_011538780.1:c.1567C=	XP_011537082.1:p.Pro523=
XM_011538781.1:c.1015C=	XP_011537083.1:p.Pro339=
XM_011538778.2:c.1666C=	XP_011537080.1:p.Pro556=
XM_011538780.2:c.1567C=	XP_011537082.1:p.Pro523=
XR_001748875.2:n.1681C=
NM_015665.6:c.1624C= MANE Select	NP_056480.1:p.Pro542=
NM_001173466.2:c.1525C=	NP_001166937.1:p.Pro509=