Canonical Allele Identifier: CA2508635368

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504133_102504134del , CM000672.2:g.102504133_102504134del	GRCh38
NC_000010.10:g.104263890_104263891del , CM000672.1:g.104263890_104263891del	GRCh37
NC_000010.9:g.104253880_104253881del	NCBI36
NG_011901.1:g.3623_3624del
NG_021338.1:g.5172_5173del , LRG_521:g.5172_5173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-20_-19del MANE Select	ENSP00000358918.4:n.-20_-19del
ENST00000369899.6:c.-20_-19del	ENSP00000358915.2:n.-20_-19del
ENST00000369902.7:c.-20_-19del	ENSP00000358918.3:n.-20_-19del
ENST00000423559.2:c.-20_-19del	ENSP00000411597.2:n.-20_-19del
NM_001178133.1:c.-20_-19del	NP_001171604.1:n.-20_-19del
NM_016169.3:c.-20_-19del , LRG_521t1:c.-20_-19del	NP_057253.2:n.-20_-19del
XM_011539858.1:c.-20_-19del	XP_011538160.1:n.-20_-19del
XM_011539859.1:c.-20_-19del	XP_011538161.1:n.-20_-19del
XM_011539860.1:c.-20_-19del	XP_011538162.1:n.-20_-19del
XM_011539861.1:c.-20_-19del	XP_011538163.1:n.-20_-19del
XM_011539863.1:c.8+1147_8+1148del	XP_011538165.1:n.8+1147_8+1148del
XM_011539864.1:c.-20_-19del	XP_011538166.1:n.-20_-19del
XM_011539858.3:c.-20_-19del	XP_011538160.1:n.-20_-19del
XM_011539860.3:c.-20_-19del	XP_011538162.1:n.-20_-19del
XM_011539861.3:c.-20_-19del	XP_011538163.1:n.-20_-19del
XM_011539863.3:c.8+1147_8+1148del	XP_011538165.1:n.8+1147_8+1148del
XM_011539864.3:c.-20_-19del	XP_011538166.1:n.-20_-19del
NM_001178133.2:c.-20_-19del	NP_001171604.1:n.-20_-19del
NM_016169.4:c.-20_-19del MANE Select	NP_057253.2:n.-20_-19del