Canonical Allele Identifier: CA2695223379
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51141016del , CM000678.2:g.51141016del GRCh38
NC_000016.9:g.51174927del , CM000678.1:g.51174927del GRCh37
NC_000016.8:g.49732428del NCBI36
NG_007990.1:g.15260del , LRG_674:g.15260del

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.1209del ENSP00000407914.2:p.Ser404AlafsTer13
ENST00000570206.2:c.918del ENSP00000456777.2:p.Ser307AlafsTer13
ENST00000685868.1:c.1209del ENSP00000509873.1:p.Ser404AlafsTer13
ENST00000690502.1:c.1209del ENSP00000510560.1:p.Ser404AlafsTer13
ENST00000251020.9:c.1209del MANE Select ENSP00000251020.4:p.Ser404AlafsTer13
ENST00000251020.8:c.1209del ENSP00000251020.4:p.Ser404AlafsTer13
ENST00000440970.5:c.918del ENSP00000407914.1:p.Ser307AlafsTer13
ENST00000566102.1:c.77-3461del ENSP00000455582.1:n.77-3461del
ENST00000570206.1:c.918del ENSP00000456777.1:p.Ser307AlafsTer13
NM_001127892.1:c.918del NP_001121364.1:p.Ser307AlafsTer13
NM_002968.2:c.1209del , LRG_674t1:c.1209del NP_002959.2:p.Ser404AlafsTer13
XM_006721241.2:c.1209del XP_006721304.1:p.Ser404AlafsTer13
XM_011523254.1:c.1209del XP_011521556.1:p.Ser404AlafsTer13
XM_011523255.1:c.1209del XP_011521557.1:p.Ser404AlafsTer13
NM_002968.3:c.1209del MANE Select NP_002959.2:p.Ser404AlafsTer13
NM_001127892.2:c.918del NP_001121364.1:p.Ser307AlafsTer13