Canonical Allele Identifier: CA385040342

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53702532G>C (hg19) ; chr12:g.53308748G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53308748G>C , CM000674.2:g.53308748G>C	GRCh38
NC_000012.11:g.53702532G>C , CM000674.1:g.53702532G>C	GRCh37
NC_000012.10:g.51988799G>C	NCBI36
NG_016775.1:g.17881C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1064C>G MANE Select	ENSP00000209873.4:p.Ser355Cys
ENST00000546562.6:n.2128C>G
ENST00000547238.6:n.1700C>G
ENST00000547520.6:n.1058C>G
ENST00000547757.2:c.113C>G	ENSP00000448020.2:p.Ser38Cys
ENST00000548880.2:n.1514C>G
ENST00000548931.6:c.584C>G	ENSP00000457518.1:p.Ser195Cys
ENST00000549450.6:n.998C>G
ENST00000552161.6:n.2020C>G
ENST00000672797.1:n.1553C>G
ENST00000672900.1:n.2006C>G
ENST00000209873.8:c.1064C>G	ENSP00000209873.4:p.Ser355Cys
ENST00000394384.7:c.965C>G	ENSP00000377908.3:p.Ser322Cys
ENST00000547520.5:n.768C>G
ENST00000548931.5:c.584C>G	ENSP00000457518.1:p.Ser195Cys
ENST00000550033.5:n.319C>G
ENST00000550286.5:c.692C>G	ENSP00000446885.1:p.Ser231Cys
ENST00000552876.5:n.1407C>G
NM_001173466.1:c.965C>G	NP_001166937.1:p.Ser322Cys
NM_015665.5:c.1064C>G	NP_056480.1:p.Ser355Cys
XM_006719617.2:c.1079C>G	XP_006719680.1:p.Ser360Cys
XM_011538777.1:c.1079C>G	XP_011537079.1:p.Ser360Cys
XM_011538778.1:c.1064C>G	XP_011537080.1:p.Ser355Cys
XM_011538779.1:c.980C>G	XP_011537081.1:p.Ser327Cys
XM_011538780.1:c.965C>G	XP_011537082.1:p.Ser322Cys
XM_011538781.1:c.413C>G	XP_011537083.1:p.Ser138Cys
XM_011538778.2:c.1064C>G	XP_011537080.1:p.Ser355Cys
XM_011538780.2:c.965C>G	XP_011537082.1:p.Ser322Cys
XR_001748875.2:n.1121C>G
NM_015665.6:c.1064C>G MANE Select	NP_056480.1:p.Ser355Cys
NM_001173466.2:c.965C>G	NP_001166937.1:p.Ser322Cys