Canonical Allele Identifier: CA913185004
Community Standard Title: NM_020436.5(SALL4):c.2425del (p.Ala809GlnfsTer?)
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51790058del , CM000682.2:g.51790058del GRCh38
NC_000020.10:g.50406597del , CM000682.1:g.50406597del GRCh37
NC_000020.9:g.49840004del NCBI36
NG_008000.1:g.17452del , LRG_675:g.17452del

Transcript Alleles

HGVS Amino-acid Change
NM_020436.5:c.2425del MANE Select NP_065169.1:p.Ala809GlnfsTer?
ENST00000217086.9:c.2425del MANE Select ENSP00000217086.4:p.Ala809GlnfsTer?
NM_001318031.1:c.1151-917del NP_001304960.1:n.1151-917del
NM_001318031.2:c.1151-917del NP_001304960.1:n.1151-917del
NM_020436.3:c.2425del , LRG_675t1:c.2425del NP_065169.1:p.Ala809GlnfsTer?
NM_020436.4:c.2425del NP_065169.1:p.Ala809GlnfsTer?
ENST00000217086.8:c.2425del ENSP00000217086.4:p.Ala809GlnfsTer?
ENST00000371539.7:c.131-917del ENSP00000360594.3:n.131-917del
ENST00000395997.3:c.1151-917del ENSP00000379319.3:n.1151-917del
XM_005260467.2:c.2119del XP_005260524.1:p.Ala707GlnfsTer?
XM_005260467.4:c.2119del XP_005260524.1:p.Ala707GlnfsTer?
XM_006723834.2:c.2119del XP_006723897.1:p.Ala707GlnfsTer?
XM_011528919.1:c.2299del XP_011527221.1:p.Ala767GlnfsTer?
XM_011528920.1:c.2119del XP_011527222.1:p.Ala707GlnfsTer?
XM_011528921.1:c.2119del XP_011527223.1:p.Ala707GlnfsTer?
XM_011528921.2:c.2119del XP_011527223.1:p.Ala707GlnfsTer?
XM_011528922.1:c.2119del XP_011527224.1:p.Ala707GlnfsTer?
XM_011528922.2:c.2119del XP_011527224.1:p.Ala707GlnfsTer?
XM_011528923.1:c.1151-917del XP_011527225.1:n.1151-917del