Canonical Allele Identifier: CA2222077767
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51136078_51136079delinsAC , CM000678.2:g.51136078_51136079delinsAC GRCh38
NC_000016.9:g.51169989_51169990delinsAC , CM000678.1:g.51169989_51169990delinsAC GRCh37
NC_000016.8:g.49727490_49727491delinsAC NCBI36
NG_007990.1:g.20194_20195delinsGT , LRG_674:g.20194_20195delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.*1033_*1034delinsGT ENSP00000407914.2:n.*1033_*1034delinsGT
ENST00000685868.1:c.*1033_*1034delinsGT ENSP00000509873.1:n.*1033_*1034delinsGT
ENST00000251020.9:c.*1033_*1034delinsGT MANE Select ENSP00000251020.4:n.*1033_*1034delinsGT
ENST00000251020.8:c.*1033_*1034delinsGT ENSP00000251020.4:n.*1033_*1034delinsGT
ENST00000440970.5:c.*1033_*1034delinsGT ENSP00000407914.1:n.*1033_*1034delinsGT
NM_001127892.1:c.*1033_*1034delinsGT NP_001121364.1:n.*1033_*1034delinsGT
NM_002968.2:c.*1033_*1034delinsGT , LRG_674t1:c.*1033_*1034delinsGT NP_002959.2:n.*1033_*1034delinsGT
XM_006721241.2:c.*1033_*1034delinsGT XP_006721304.1:n.*1033_*1034delinsGT
XM_011523254.1:c.*1033_*1034delinsGT XP_011521556.1:n.*1033_*1034delinsGT
XM_011523255.1:c.*1033_*1034delinsGT XP_011521557.1:n.*1033_*1034delinsGT
NM_002968.3:c.*1033_*1034delinsGT MANE Select NP_002959.2:n.*1033_*1034delinsGT
NM_001127892.2:c.*1033_*1034delinsGT NP_001121364.1:n.*1033_*1034delinsGT