Canonical Allele Identifier: CA595216440

Gene: SUFU

Linked Data

• dbSNP Id: rs1279453526
• gnomAD v2: 10-104263784-C-G
• gnomAD v3: 10-102504027-C-G
• gnomAD v4: 10-102504027-C-G
• MyVariant Identifiers: chr10:g.104263784C>G (hg19) ; chr10:g.102504027C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504027C>G , CM000672.2:g.102504027C>G	GRCh38
NC_000010.10:g.104263784C>G , CM000672.1:g.104263784C>G	GRCh37
NC_000010.9:g.104253774C>G	NCBI36
NG_011901.1:g.3729G>C
NG_021338.1:g.5066C>G , LRG_521:g.5066C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-126C>G MANE Select	ENSP00000358918.4:n.-126C>G
ENST00000369899.6:c.-126C>G	ENSP00000358915.2:n.-126C>G
ENST00000369902.7:c.-126C>G	ENSP00000358918.3:n.-126C>G
NM_001178133.1:c.-126C>G	NP_001171604.1:n.-126C>G
NM_016169.3:c.-126C>G , LRG_521t1:c.-126C>G	NP_057253.2:n.-126C>G
XM_011539858.1:c.-126C>G	XP_011538160.1:n.-126C>G
XM_011539859.1:c.-29-97C>G	XP_011538161.1:n.-29-97C>G
XM_011539860.1:c.-126C>G	XP_011538162.1:n.-126C>G
XM_011539863.1:c.8+1041C>G	XP_011538165.1:n.8+1041C>G
XM_011539858.3:c.-126C>G	XP_011538160.1:n.-126C>G
XM_011539860.3:c.-126C>G	XP_011538162.1:n.-126C>G
XM_011539861.3:c.-126C>G	XP_011538163.1:n.-126C>G
XM_011539863.3:c.8+1041C>G	XP_011538165.1:n.8+1041C>G
XM_011539864.3:c.-126C>G	XP_011538166.1:n.-126C>G
NM_001178133.2:c.-126C>G	NP_001171604.1:n.-126C>G
NM_016169.4:c.-126C>G MANE Select	NP_057253.2:n.-126C>G