Canonical Allele Identifier: CA5667973

Gene: SUFU

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102627162T>C , CM000672.2:g.102627162T>C	GRCh38
NC_000010.10:g.104386919T>C , CM000672.1:g.104386919T>C	GRCh37
NC_000010.9:g.104376909T>C	NCBI36
NG_021338.1:g.128201T>C , LRG_521:g.128201T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_016169.4:c.1297-13T>C MANE Select	NP_057253.2:n.1297-13T>C
ENST00000369902.8:c.1297-13T>C MANE Select	ENSP00000358918.4:n.1297-13T>C
NM_016169.3:c.1297-13T>C , LRG_521t1:c.1297-13T>C	NP_057253.2:n.1297-13T>C
ENST00000369902.7:c.1297-13T>C	ENSP00000358918.3:n.1297-13T>C
XM_011539858.1:c.1426-13T>C	XP_011538160.1:n.1426-13T>C
XM_011539858.3:c.1426-13T>C	XP_011538160.1:n.1426-13T>C
XM_011539859.1:c.1426-13T>C	XP_011538161.1:n.1426-13T>C
XM_011539860.1:c.1423-13T>C	XP_011538162.1:n.1423-13T>C
XM_011539860.3:c.1423-13T>C	XP_011538162.1:n.1423-13T>C
XM_011539861.1:c.1300-13T>C	XP_011538163.1:n.1300-13T>C
XM_011539861.3:c.1300-13T>C	XP_011538163.1:n.1300-13T>C
XM_011539862.1:c.1348-13T>C	XP_011538164.1:n.1348-13T>C
XM_011539863.1:c.1252-13T>C	XP_011538165.1:n.1252-13T>C
XM_011539863.3:c.1252-13T>C	XP_011538165.1:n.1252-13T>C
XM_017016323.1:c.1348-13T>C	XP_016871812.1:n.1348-13T>C