Canonical Allele Identifier: CA377886306

Gene: SUFU

Linked Data

• ClinVar Variation Id: 2937768
• ClinVar RCV Id: RCV003794398
• MyVariant Identifiers: chr10:g.104263971C>T (hg19) ; chr10:g.102504214C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504214C>T , CM000672.2:g.102504214C>T	GRCh38
NC_000010.10:g.104263971C>T , CM000672.1:g.104263971C>T	GRCh37
NC_000010.9:g.104253961C>T	NCBI36
NG_011901.1:g.3542G>A
NG_021338.1:g.5253C>T , LRG_521:g.5253C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.62C>T MANE Select	ENSP00000358918.4:p.Thr21Ile
ENST00000369899.6:c.62C>T	ENSP00000358915.2:p.Thr21Ile
ENST00000369902.7:c.62C>T	ENSP00000358918.3:p.Thr21Ile
ENST00000423559.2:c.62C>T	ENSP00000411597.2:p.Thr21Ile
NM_001178133.1:c.62C>T	NP_001171604.1:p.Thr21Ile
NM_016169.3:c.62C>T , LRG_521t1:c.62C>T	NP_057253.2:p.Thr21Ile
XM_011539858.1:c.62C>T	XP_011538160.1:p.Thr21Ile
XM_011539859.1:c.62C>T	XP_011538161.1:p.Thr21Ile
XM_011539860.1:c.62C>T	XP_011538162.1:p.Thr21Ile
XM_011539861.1:c.62C>T	XP_011538163.1:p.Thr21Ile
XM_011539863.1:c.8+1228C>T	XP_011538165.1:n.8+1228C>T
XM_011539864.1:c.62C>T	XP_011538166.1:p.Thr21Ile
XM_011539858.3:c.62C>T	XP_011538160.1:p.Thr21Ile
XM_011539860.3:c.62C>T	XP_011538162.1:p.Thr21Ile
XM_011539861.3:c.62C>T	XP_011538163.1:p.Thr21Ile
XM_011539863.3:c.8+1228C>T	XP_011538165.1:n.8+1228C>T
XM_011539864.3:c.62C>T	XP_011538166.1:p.Thr21Ile
NM_001178133.2:c.62C>T	NP_001171604.1:p.Thr21Ile
NM_016169.4:c.62C>T MANE Select	NP_057253.2:p.Thr21Ile