Canonical Allele Identifier: CA5668006

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102630145C>T , CM000672.2:g.102630145C>T	GRCh38
NC_000010.10:g.104389902C>T , CM000672.1:g.104389902C>T	GRCh37
NC_000010.9:g.104379892C>T	NCBI36
NG_021338.1:g.131184C>T , LRG_521:g.131184C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1445C>T MANE Select	NP_057253.2:p.Pro482Leu
ENST00000369902.8:c.1445C>T MANE Select	ENSP00000358918.4:p.Pro482Leu
NM_016169.3:c.1445C>T , LRG_521t1:c.1445C>T	NP_057253.2:p.Pro482Leu
ENST00000369902.7:c.1445C>T	ENSP00000358918.3:p.Pro482Leu
XM_011539858.1:c.1574C>T	XP_011538160.1:p.Pro525Leu
XM_011539858.3:c.1574C>T	XP_011538160.1:p.Pro525Leu
XM_011539859.1:c.1574C>T	XP_011538161.1:p.Pro525Leu
XM_011539860.1:c.1571C>T	XP_011538162.1:p.Pro524Leu
XM_011539860.3:c.1571C>T	XP_011538162.1:p.Pro524Leu
XM_011539861.1:c.1448C>T	XP_011538163.1:p.Pro483Leu
XM_011539861.3:c.1448C>T	XP_011538163.1:p.Pro483Leu
XM_011539862.1:c.1496C>T	XP_011538164.1:p.Pro499Leu
XM_011539863.1:c.1400C>T	XP_011538165.1:p.Pro467Leu
XM_011539863.3:c.1400C>T	XP_011538165.1:p.Pro467Leu
XM_017016323.1:c.1496C>T	XP_016871812.1:p.Pro499Leu