Canonical Allele Identifier: CA212237974

Gene: SUFU

Linked Data

• dbSNP Id: rs1013153844
• gnomAD v2: 10-104263780-G-A
• gnomAD v3: 10-102504023-G-A
• gnomAD v4: 10-102504023-G-A
• MyVariant Identifiers: chr10:g.104263780G>A (hg19) ; chr10:g.102504023G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504023G>A , CM000672.2:g.102504023G>A	GRCh38
NC_000010.10:g.104263780G>A , CM000672.1:g.104263780G>A	GRCh37
NC_000010.9:g.104253770G>A	NCBI36
NG_011901.1:g.3733C>T
NG_021338.1:g.5062G>A , LRG_521:g.5062G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-130G>A MANE Select	ENSP00000358918.4:n.-130G>A
ENST00000369899.6:c.-130G>A	ENSP00000358915.2:n.-130G>A
ENST00000369902.7:c.-130G>A	ENSP00000358918.3:n.-130G>A
NM_001178133.1:c.-130G>A	NP_001171604.1:n.-130G>A
NM_016169.3:c.-130G>A , LRG_521t1:c.-130G>A	NP_057253.2:n.-130G>A
XM_011539858.1:c.-130G>A	XP_011538160.1:n.-130G>A
XM_011539859.1:c.-29-101G>A	XP_011538161.1:n.-29-101G>A
XM_011539860.1:c.-130G>A	XP_011538162.1:n.-130G>A
XM_011539863.1:c.8+1037G>A	XP_011538165.1:n.8+1037G>A
XM_011539858.3:c.-130G>A	XP_011538160.1:n.-130G>A
XM_011539860.3:c.-130G>A	XP_011538162.1:n.-130G>A
XM_011539861.3:c.-130G>A	XP_011538163.1:n.-130G>A
XM_011539863.3:c.8+1037G>A	XP_011538165.1:n.8+1037G>A
XM_011539864.3:c.-130G>A	XP_011538166.1:n.-130G>A
NM_001178133.2:c.-130G>A	NP_001171604.1:n.-130G>A
NM_016169.4:c.-130G>A MANE Select	NP_057253.2:n.-130G>A