Canonical Allele Identifier: CA385034552

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53701296G>C (hg19) ; chr12:g.53307512G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53307512G>C , CM000674.2:g.53307512G>C	GRCh38
NC_000012.11:g.53701296G>C , CM000674.1:g.53701296G>C	GRCh37
NC_000012.10:g.51987563G>C	NCBI36
NG_016775.1:g.19117C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1618C>G MANE Select	ENSP00000209873.4:p.His540Asp
ENST00000546562.6:n.2682C>G
ENST00000547757.2:c.*536C>G	ENSP00000448020.2:n.*536C>G
ENST00000548931.6:c.1053C>G	ENSP00000457518.1:p.Pro351=
ENST00000549450.6:n.1552C>G
ENST00000209873.8:c.1618C>G	ENSP00000209873.4:p.His540Asp
ENST00000394384.7:c.1519C>G	ENSP00000377908.3:p.His507Asp
ENST00000548931.5:c.1053C>G	ENSP00000457518.1:p.Pro351=
ENST00000550286.5:c.1246C>G	ENSP00000446885.1:p.His416Asp
ENST00000552876.5:n.1961C>G
NM_001173466.1:c.1519C>G	NP_001166937.1:p.His507Asp
NM_015665.5:c.1618C>G	NP_056480.1:p.His540Asp
XM_006719617.2:c.1633C>G	XP_006719680.1:p.His545Asp
XM_011538777.1:c.1675C>G	XP_011537079.1:p.His559Asp
XM_011538778.1:c.1660C>G	XP_011537080.1:p.His554Asp
XM_011538779.1:c.1576C>G	XP_011537081.1:p.His526Asp
XM_011538780.1:c.1561C>G	XP_011537082.1:p.His521Asp
XM_011538781.1:c.1009C>G	XP_011537083.1:p.His337Asp
XM_011538778.2:c.1660C>G	XP_011537080.1:p.His554Asp
XM_011538780.2:c.1561C>G	XP_011537082.1:p.His521Asp
XR_001748875.2:n.1675C>G
NM_015665.6:c.1618C>G MANE Select	NP_056480.1:p.His540Asp
NM_001173466.2:c.1519C>G	NP_001166937.1:p.His507Asp