Canonical Allele Identifier: CA2610693828

Gene: SUFU

Linked Data

• gnomAD v4: 10-102504001-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102504001A>T , CM000672.2:g.102504001A>T	GRCh38
NC_000010.10:g.104263758A>T , CM000672.1:g.104263758A>T	GRCh37
NC_000010.9:g.104253748A>T	NCBI36
NG_011901.1:g.3755T>A
NG_021338.1:g.5040A>T , LRG_521:g.5040A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369902.8:c.-152A>T MANE Select	ENSP00000358918.4:n.-152A>T
ENST00000369902.7:c.-152A>T	ENSP00000358918.3:n.-152A>T
NM_001178133.1:c.-152A>T	NP_001171604.1:n.-152A>T
NM_016169.3:c.-152A>T , LRG_521t1:c.-152A>T	NP_057253.2:n.-152A>T
XM_011539858.1:c.-152A>T	XP_011538160.1:n.-152A>T
XM_011539859.1:c.-29-123A>T	XP_011538161.1:n.-29-123A>T
XM_011539860.1:c.-152A>T	XP_011538162.1:n.-152A>T
XM_011539863.1:c.8+1015A>T	XP_011538165.1:n.8+1015A>T
XM_011539858.3:c.-152A>T	XP_011538160.1:n.-152A>T
XM_011539860.3:c.-152A>T	XP_011538162.1:n.-152A>T
XM_011539861.3:c.-152A>T	XP_011538163.1:n.-152A>T
XM_011539863.3:c.8+1015A>T	XP_011538165.1:n.8+1015A>T
XM_011539864.3:c.-152A>T	XP_011538166.1:n.-152A>T
NM_001178133.2:c.-152A>T	NP_001171604.1:n.-152A>T
NM_016169.4:c.-152A>T MANE Select	NP_057253.2:n.-152A>T