Canonical Allele Identifier: CA2513009512

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504064T>G , CM000672.2:g.102504064T>G	GRCh38
NC_000010.10:g.104263821T>G , CM000672.1:g.104263821T>G	GRCh37
NC_000010.9:g.104253811T>G	NCBI36
NG_011901.1:g.3692A>C
NG_021338.1:g.5103T>G , LRG_521:g.5103T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-89T>G MANE Select	ENSP00000358918.4:n.-89T>G
ENST00000369899.6:c.-89T>G	ENSP00000358915.2:n.-89T>G
ENST00000369902.7:c.-89T>G	ENSP00000358918.3:n.-89T>G
NM_001178133.1:c.-89T>G	NP_001171604.1:n.-89T>G
NM_016169.3:c.-89T>G , LRG_521t1:c.-89T>G	NP_057253.2:n.-89T>G
XM_011539858.1:c.-89T>G	XP_011538160.1:n.-89T>G
XM_011539859.1:c.-29-60T>G	XP_011538161.1:n.-29-60T>G
XM_011539860.1:c.-89T>G	XP_011538162.1:n.-89T>G
XM_011539863.1:c.8+1078T>G	XP_011538165.1:n.8+1078T>G
XM_011539858.3:c.-89T>G	XP_011538160.1:n.-89T>G
XM_011539860.3:c.-89T>G	XP_011538162.1:n.-89T>G
XM_011539861.3:c.-89T>G	XP_011538163.1:n.-89T>G
XM_011539863.3:c.8+1078T>G	XP_011538165.1:n.8+1078T>G
XM_011539864.3:c.-89T>G	XP_011538166.1:n.-89T>G
NM_001178133.2:c.-89T>G	NP_001171604.1:n.-89T>G
NM_016169.4:c.-89T>G MANE Select	NP_057253.2:n.-89T>G