Canonical Allele Identifier: CA5667982

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102627203A>G , CM000672.2:g.102627203A>G	GRCh38
NC_000010.10:g.104386960A>G , CM000672.1:g.104386960A>G	GRCh37
NC_000010.9:g.104376950A>G	NCBI36
NG_021338.1:g.128242A>G , LRG_521:g.128242A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1325A>G MANE Select	NP_057253.2:p.Lys442Arg
ENST00000369902.8:c.1325A>G MANE Select	ENSP00000358918.4:p.Lys442Arg
NM_016169.3:c.1325A>G , LRG_521t1:c.1325A>G	NP_057253.2:p.Lys442Arg
ENST00000369902.7:c.1325A>G	ENSP00000358918.3:p.Lys442Arg
XM_011539858.1:c.1454A>G	XP_011538160.1:p.Lys485Arg
XM_011539858.3:c.1454A>G	XP_011538160.1:p.Lys485Arg
XM_011539859.1:c.1454A>G	XP_011538161.1:p.Lys485Arg
XM_011539860.1:c.1451A>G	XP_011538162.1:p.Lys484Arg
XM_011539860.3:c.1451A>G	XP_011538162.1:p.Lys484Arg
XM_011539861.1:c.1328A>G	XP_011538163.1:p.Lys443Arg
XM_011539861.3:c.1328A>G	XP_011538163.1:p.Lys443Arg
XM_011539862.1:c.1376A>G	XP_011538164.1:p.Lys459Arg
XM_011539863.1:c.1280A>G	XP_011538165.1:p.Lys427Arg
XM_011539863.3:c.1280A>G	XP_011538165.1:p.Lys427Arg
XM_017016323.1:c.1376A>G	XP_016871812.1:p.Lys459Arg