Canonical Allele Identifier: CA385036875

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701439G>C (hg19) ; chr12:g.53307655G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307655G>C , CM000674.2:g.53307655G>C	GRCh38
NC_000012.11:g.53701439G>C , CM000674.1:g.53701439G>C	GRCh37
NC_000012.10:g.51987706G>C	NCBI36
NG_016775.1:g.18974C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1475C>G MANE Select	ENSP00000209873.4:p.Pro492Arg
ENST00000546562.6:n.2539C>G
ENST00000547238.6:n.2111C>G
ENST00000547520.6:n.1591C>G
ENST00000547757.2:c.*393C>G	ENSP00000448020.2:n.*393C>G
ENST00000548880.2:n.1925C>G
ENST00000548931.6:c.910C>G	ENSP00000457518.1:p.His304Asp
ENST00000549450.6:n.1409C>G
ENST00000552161.6:n.2553C>G
ENST00000672797.1:n.1964C>G
ENST00000209873.8:c.1475C>G	ENSP00000209873.4:p.Pro492Arg
ENST00000394384.7:c.1376C>G	ENSP00000377908.3:p.Pro459Arg
ENST00000548931.5:c.910C>G	ENSP00000457518.1:p.His304Asp
ENST00000550286.5:c.1103C>G	ENSP00000446885.1:p.Pro368Arg
ENST00000552876.5:n.1818C>G
NM_001173466.1:c.1376C>G	NP_001166937.1:p.Pro459Arg
NM_015665.5:c.1475C>G	NP_056480.1:p.Pro492Arg
XM_006719617.2:c.1490C>G	XP_006719680.1:p.Pro497Arg
XM_011538777.1:c.1532C>G	XP_011537079.1:p.Pro511Arg
XM_011538778.1:c.1517C>G	XP_011537080.1:p.Pro506Arg
XM_011538779.1:c.1433C>G	XP_011537081.1:p.Pro478Arg
XM_011538780.1:c.1418C>G	XP_011537082.1:p.Pro473Arg
XM_011538781.1:c.866C>G	XP_011537083.1:p.Pro289Arg
XM_011538778.2:c.1517C>G	XP_011537080.1:p.Pro506Arg
XM_011538780.2:c.1418C>G	XP_011537082.1:p.Pro473Arg
XR_001748875.2:n.1532C>G
NM_015665.6:c.1475C>G MANE Select	NP_056480.1:p.Pro492Arg
NM_001173466.2:c.1376C>G	NP_001166937.1:p.Pro459Arg