Canonical Allele Identifier: CA385035286

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701400G>T (hg19) ; chr12:g.53307616G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307616G>T , CM000674.2:g.53307616G>T	GRCh38
NC_000012.11:g.53701400G>T , CM000674.1:g.53701400G>T	GRCh37
NC_000012.10:g.51987667G>T	NCBI36
NG_016775.1:g.19013C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1514C>A MANE Select	ENSP00000209873.4:p.Pro505His
ENST00000546562.6:n.2578C>A
ENST00000547238.6:n.2150C>A
ENST00000547520.6:n.1630C>A
ENST00000547757.2:c.*432C>A	ENSP00000448020.2:n.*432C>A
ENST00000548931.6:c.949C>A	ENSP00000457518.1:p.Leu317Met
ENST00000549450.6:n.1448C>A
ENST00000672797.1:n.2003C>A
ENST00000209873.8:c.1514C>A	ENSP00000209873.4:p.Pro505His
ENST00000394384.7:c.1415C>A	ENSP00000377908.3:p.Pro472His
ENST00000548931.5:c.949C>A	ENSP00000457518.1:p.Leu317Met
ENST00000550286.5:c.1142C>A	ENSP00000446885.1:p.Pro381His
ENST00000552876.5:n.1857C>A
NM_001173466.1:c.1415C>A	NP_001166937.1:p.Pro472His
NM_015665.5:c.1514C>A	NP_056480.1:p.Pro505His
XM_006719617.2:c.1529C>A	XP_006719680.1:p.Pro510His
XM_011538777.1:c.1571C>A	XP_011537079.1:p.Pro524His
XM_011538778.1:c.1556C>A	XP_011537080.1:p.Pro519His
XM_011538779.1:c.1472C>A	XP_011537081.1:p.Pro491His
XM_011538780.1:c.1457C>A	XP_011537082.1:p.Pro486His
XM_011538781.1:c.905C>A	XP_011537083.1:p.Pro302His
XM_011538778.2:c.1556C>A	XP_011537080.1:p.Pro519His
XM_011538780.2:c.1457C>A	XP_011537082.1:p.Pro486His
XR_001748875.2:n.1571C>A
NM_015665.6:c.1514C>A MANE Select	NP_056480.1:p.Pro505His
NM_001173466.2:c.1415C>A	NP_001166937.1:p.Pro472His