Canonical Allele Identifier: CA377889200
Community Standard Title: NM_016169.4(SUFU):c.306C>A (p.Asn102Lys)
Gene: SUFU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102509292C>A , CM000672.2:g.102509292C>A GRCh38
NC_000010.10:g.104269049C>A , CM000672.1:g.104269049C>A GRCh37
NC_000010.9:g.104259039C>A NCBI36
NG_021338.1:g.10331C>A , LRG_521:g.10331C>A

Transcript Alleles

HGVS Amino-acid Change
NM_016169.4:c.306C>A MANE Select NP_057253.2:p.Asn102Lys
ENST00000369902.8:c.306C>A MANE Select ENSP00000358918.4:p.Asn102Lys
NM_001178133.1:c.306C>A NP_001171604.1:p.Asn102Lys
NM_001178133.2:c.306C>A NP_001171604.1:p.Asn102Lys
NM_016169.3:c.306C>A , LRG_521t1:c.306C>A NP_057253.2:p.Asn102Lys
ENST00000369899.6:c.306C>A ENSP00000358915.2:p.Asn102Lys
ENST00000369902.7:c.306C>A ENSP00000358918.3:p.Asn102Lys
ENST00000423559.2:c.306C>A ENSP00000411597.2:p.Asn102Lys
XM_011539858.1:c.306C>A XP_011538160.1:p.Asn102Lys
XM_011539858.3:c.306C>A XP_011538160.1:p.Asn102Lys
XM_011539859.1:c.306C>A XP_011538161.1:p.Asn102Lys
XM_011539860.1:c.306C>A XP_011538162.1:p.Asn102Lys
XM_011539860.3:c.306C>A XP_011538162.1:p.Asn102Lys
XM_011539861.1:c.306C>A XP_011538163.1:p.Asn102Lys
XM_011539861.3:c.306C>A XP_011538163.1:p.Asn102Lys
XM_011539862.1:c.228C>A XP_011538164.1:p.Asn76Lys
XM_011539863.1:c.132C>A XP_011538165.1:p.Asn44Lys
XM_011539863.3:c.132C>A XP_011538165.1:p.Asn44Lys
XM_011539864.1:c.306C>A XP_011538166.1:p.Asn102Lys
XM_011539864.3:c.306C>A XP_011538166.1:p.Asn102Lys
XM_017016323.1:c.228C>A XP_016871812.1:p.Asn76Lys