Canonical Allele Identifier: CA595216451

Gene: SUFU

Linked Data

• dbSNP Id: rs1369720313
• gnomAD v2: 10-104263869-T-C
• gnomAD v4: 10-102504112-T-C
• MyVariant Identifiers: chr10:g.104263869T>C (hg19) ; chr10:g.102504112T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504112T>C , CM000672.2:g.102504112T>C	GRCh38
NC_000010.10:g.104263869T>C , CM000672.1:g.104263869T>C	GRCh37
NC_000010.9:g.104253859T>C	NCBI36
NG_011901.1:g.3644A>G
NG_021338.1:g.5151T>C , LRG_521:g.5151T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369902.8:c.-41T>C MANE Select	ENSP00000358918.4:n.-41T>C
ENST00000369899.6:c.-41T>C	ENSP00000358915.2:n.-41T>C
ENST00000369902.7:c.-41T>C	ENSP00000358918.3:n.-41T>C
ENST00000423559.2:c.-41T>C	ENSP00000411597.2:n.-41T>C
NM_001178133.1:c.-41T>C	NP_001171604.1:n.-41T>C
NM_016169.3:c.-41T>C , LRG_521t1:c.-41T>C	NP_057253.2:n.-41T>C
XM_011539858.1:c.-41T>C	XP_011538160.1:n.-41T>C
XM_011539859.1:c.-29-12T>C	XP_011538161.1:n.-29-12T>C
XM_011539860.1:c.-41T>C	XP_011538162.1:n.-41T>C
XM_011539863.1:c.8+1126T>C	XP_011538165.1:n.8+1126T>C
XM_011539858.3:c.-41T>C	XP_011538160.1:n.-41T>C
XM_011539860.3:c.-41T>C	XP_011538162.1:n.-41T>C
XM_011539861.3:c.-41T>C	XP_011538163.1:n.-41T>C
XM_011539863.3:c.8+1126T>C	XP_011538165.1:n.8+1126T>C
XM_011539864.3:c.-41T>C	XP_011538166.1:n.-41T>C
NM_001178133.2:c.-41T>C	NP_001171604.1:n.-41T>C
NM_016169.4:c.-41T>C MANE Select	NP_057253.2:n.-41T>C