Canonical Allele Identifier: CA2546742615

Gene: SUFU

Linked Data

• gnomAD v4: 10-102504122-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504122A>G , CM000672.2:g.102504122A>G	GRCh38
NC_000010.10:g.104263879A>G , CM000672.1:g.104263879A>G	GRCh37
NC_000010.9:g.104253869A>G	NCBI36
NG_011901.1:g.3634T>C
NG_021338.1:g.5161A>G , LRG_521:g.5161A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000369902.8:c.-31A>G MANE Select	ENSP00000358918.4:n.-31A>G
ENST00000369899.6:c.-31A>G	ENSP00000358915.2:n.-31A>G
ENST00000369902.7:c.-31A>G	ENSP00000358918.3:n.-31A>G
ENST00000423559.2:c.-31A>G	ENSP00000411597.2:n.-31A>G
NM_001178133.1:c.-31A>G	NP_001171604.1:n.-31A>G
NM_016169.3:c.-31A>G , LRG_521t1:c.-31A>G	NP_057253.2:n.-31A>G
XM_011539858.1:c.-31A>G	XP_011538160.1:n.-31A>G
XM_011539859.1:c.-29-2A>G	XP_011538161.1:n.-29-2A>G
XM_011539860.1:c.-31A>G	XP_011538162.1:n.-31A>G
XM_011539863.1:c.8+1136A>G	XP_011538165.1:n.8+1136A>G
XM_011539858.3:c.-31A>G	XP_011538160.1:n.-31A>G
XM_011539860.3:c.-31A>G	XP_011538162.1:n.-31A>G
XM_011539861.3:c.-31A>G	XP_011538163.1:n.-31A>G
XM_011539863.3:c.8+1136A>G	XP_011538165.1:n.8+1136A>G
XM_011539864.3:c.-31A>G	XP_011538166.1:n.-31A>G
NM_001178133.2:c.-31A>G	NP_001171604.1:n.-31A>G
NM_016169.4:c.-31A>G MANE Select	NP_057253.2:n.-31A>G