Canonical Allele Identifier: CA385040529

Gene: AAAS

Linked Data

• MyVariant Identifiers: chr12:g.53702554A>T (hg19) ; chr12:g.53308770A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53308770A>T , CM000674.2:g.53308770A>T	GRCh38
NC_000012.11:g.53702554A>T , CM000674.1:g.53702554A>T	GRCh37
NC_000012.10:g.51988821A>T	NCBI36
NG_016775.1:g.17859T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209873.9:c.1042T>A MANE Select	ENSP00000209873.4:p.Leu348Met
ENST00000546562.6:n.2106T>A
ENST00000547238.6:n.1678T>A
ENST00000547520.6:n.1036T>A
ENST00000547757.2:c.91T>A	ENSP00000448020.2:p.Leu31Met
ENST00000548880.2:n.1492T>A
ENST00000548931.6:c.562T>A	ENSP00000457518.1:p.Leu188Met
ENST00000549450.6:n.976T>A
ENST00000552161.6:n.1998T>A
ENST00000672797.1:n.1531T>A
ENST00000672900.1:n.1984T>A
ENST00000209873.8:c.1042T>A	ENSP00000209873.4:p.Leu348Met
ENST00000394384.7:c.943T>A	ENSP00000377908.3:p.Leu315Met
ENST00000547520.5:n.746T>A
ENST00000548931.5:c.562T>A	ENSP00000457518.1:p.Leu188Met
ENST00000550033.5:n.297T>A
ENST00000550286.5:c.670T>A	ENSP00000446885.1:p.Leu224Met
ENST00000552876.5:n.1385T>A
NM_001173466.1:c.943T>A	NP_001166937.1:p.Leu315Met
NM_015665.5:c.1042T>A	NP_056480.1:p.Leu348Met
XM_006719617.2:c.1057T>A	XP_006719680.1:p.Leu353Met
XM_006719619.2:c.*52T>A	XP_006719682.1:n.*52T>A
XM_011538777.1:c.1057T>A	XP_011537079.1:p.Leu353Met
XM_011538778.1:c.1042T>A	XP_011537080.1:p.Leu348Met
XM_011538779.1:c.958T>A	XP_011537081.1:p.Leu320Met
XM_011538780.1:c.943T>A	XP_011537082.1:p.Leu315Met
XM_011538781.1:c.391T>A	XP_011537083.1:p.Leu131Met
XM_011538778.2:c.1042T>A	XP_011537080.1:p.Leu348Met
XM_011538780.2:c.943T>A	XP_011537082.1:p.Leu315Met
XR_001748875.2:n.1099T>A
NM_015665.6:c.1042T>A MANE Select	NP_056480.1:p.Leu348Met
NM_001173466.2:c.943T>A	NP_001166937.1:p.Leu315Met