Canonical Allele Identifier: CA385034433

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701280T>C (hg19) ; chr12:g.53307496T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307496T>C , CM000674.2:g.53307496T>C	GRCh38
NC_000012.11:g.53701280T>C , CM000674.1:g.53701280T>C	GRCh37
NC_000012.10:g.51987547T>C	NCBI36
NG_016775.1:g.19133A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1634A>G MANE Select	ENSP00000209873.4:p.His545Arg
ENST00000547757.2:c.*552A>G	ENSP00000448020.2:n.*552A>G
ENST00000548931.6:c.1069A>G	ENSP00000457518.1:p.Thr357Ala
ENST00000549450.6:n.1568A>G
ENST00000209873.8:c.1634A>G	ENSP00000209873.4:p.His545Arg
ENST00000394384.7:c.1535A>G	ENSP00000377908.3:p.His512Arg
ENST00000548931.5:c.1069A>G	ENSP00000457518.1:p.Thr357Ala
ENST00000550286.5:c.1262A>G	ENSP00000446885.1:p.His421Arg
ENST00000552876.5:n.1977A>G
NM_001173466.1:c.1535A>G	NP_001166937.1:p.His512Arg
NM_015665.5:c.1634A>G	NP_056480.1:p.His545Arg
XM_006719617.2:c.1649A>G	XP_006719680.1:p.His550Arg
XM_011538777.1:c.1691A>G	XP_011537079.1:p.His564Arg
XM_011538778.1:c.1676A>G	XP_011537080.1:p.His559Arg
XM_011538779.1:c.1592A>G	XP_011537081.1:p.His531Arg
XM_011538780.1:c.1577A>G	XP_011537082.1:p.His526Arg
XM_011538781.1:c.1025A>G	XP_011537083.1:p.His342Arg
XM_011538778.2:c.1676A>G	XP_011537080.1:p.His559Arg
XM_011538780.2:c.1577A>G	XP_011537082.1:p.His526Arg
XR_001748875.2:n.1691A>G
NM_015665.6:c.1634A>G MANE Select	NP_056480.1:p.His545Arg
NM_001173466.2:c.1535A>G	NP_001166937.1:p.His512Arg