Canonical Allele Identifier: CA377902943
Community Standard Title: NM_016169.4(SUFU):c.318-1G>C
Gene: SUFU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102549969G>C , CM000672.2:g.102549969G>C GRCh38
NC_000010.10:g.104309726G>C , CM000672.1:g.104309726G>C GRCh37
NC_000010.9:g.104299716G>C NCBI36
NG_021338.1:g.51008G>C , LRG_521:g.51008G>C

Transcript Alleles

HGVS Amino-acid Change
NM_016169.4:c.318-1G>C MANE Select NP_057253.2:n.318-1G>C
ENST00000369902.8:c.318-1G>C MANE Select ENSP00000358918.4:n.318-1G>C
NM_001178133.1:c.318-1G>C NP_001171604.1:n.318-1G>C
NM_001178133.2:c.318-1G>C NP_001171604.1:n.318-1G>C
NM_016169.3:c.318-1G>C , LRG_521t1:c.318-1G>C NP_057253.2:n.318-1G>C
ENST00000369899.6:c.318-1G>C ENSP00000358915.2:n.318-1G>C
ENST00000369902.7:c.318-1G>C ENSP00000358918.3:n.318-1G>C
ENST00000423559.2:c.318-1G>C ENSP00000411597.2:n.318-1G>C
XM_011539858.1:c.318-1G>C XP_011538160.1:n.318-1G>C
XM_011539858.3:c.318-1G>C XP_011538160.1:n.318-1G>C
XM_011539859.1:c.318-1G>C XP_011538161.1:n.318-1G>C
XM_011539860.1:c.318-1G>C XP_011538162.1:n.318-1G>C
XM_011539860.3:c.318-1G>C XP_011538162.1:n.318-1G>C
XM_011539861.1:c.318-1G>C XP_011538163.1:n.318-1G>C
XM_011539861.3:c.318-1G>C XP_011538163.1:n.318-1G>C
XM_011539862.1:c.240-1G>C XP_011538164.1:n.240-1G>C
XM_011539863.1:c.144-1G>C XP_011538165.1:n.144-1G>C
XM_011539863.3:c.144-1G>C XP_011538165.1:n.144-1G>C
XM_011539864.1:c.318-1G>C XP_011538166.1:n.318-1G>C
XM_011539864.3:c.318-1G>C XP_011538166.1:n.318-1G>C
XM_017016323.1:c.240-1G>C XP_016871812.1:n.240-1G>C