Canonical Allele Identifier: CA2633181094
Gene: SALL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51139275_51139277del , CM000678.2:g.51139275_51139277del GRCh38
NC_000016.9:g.51173186_51173188del , CM000678.1:g.51173186_51173188del GRCh37
NC_000016.8:g.49730687_49730689del NCBI36
NG_007990.1:g.17000_17002del , LRG_674:g.17000_17002del

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.2949_2951del ENSP00000407914.2:p.Glu983del
ENST00000570206.2:c.2658_2660del ENSP00000456777.2:p.Glu886del
ENST00000685868.1:c.2949_2951del ENSP00000509873.1:p.Glu983del
ENST00000690502.1:c.2949_2951del ENSP00000510560.1:p.Glu983del
ENST00000251020.9:c.2949_2951del MANE Select ENSP00000251020.4:p.Glu983del
ENST00000251020.8:c.2949_2951del ENSP00000251020.4:p.Glu983del
ENST00000440970.5:c.2658_2660del ENSP00000407914.1:p.Glu886del
ENST00000566102.1:c.77-1721_77-1719del ENSP00000455582.1:n.77-1721_77-1719del
ENST00000570206.1:c.2658_2660del ENSP00000456777.1:p.Glu886del
NM_001127892.1:c.2658_2660del NP_001121364.1:p.Glu886del
NM_002968.2:c.2949_2951del , LRG_674t1:c.2949_2951del NP_002959.2:p.Glu983del
XM_006721241.2:c.2949_2951del XP_006721304.1:p.Glu983del
XM_011523254.1:c.2949_2951del XP_011521556.1:p.Glu983del
XM_011523255.1:c.2949_2951del XP_011521557.1:p.Glu983del
NM_002968.3:c.2949_2951del MANE Select NP_002959.2:p.Glu983del
NM_001127892.2:c.2658_2660del NP_001121364.1:p.Glu886del