Canonical Allele Identifier: CA2222022772
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51141729_51141750delinsAGCTGCCGCCGCCGCCGCTGCT , CM000678.2:g.51141729_51141750delinsAGCTGCCGCCGCCGCCGCTGCT GRCh38
NC_000016.9:g.51175640_51175661delinsAGCTGCCGCCGCCGCCGCTGCT , CM000678.1:g.51175640_51175661delinsAGCTGCCGCCGCCGCCGCTGCT GRCh37
NC_000016.8:g.49733141_49733162delinsAGCTGCCGCCGCCGCCGCTGCT NCBI36
NG_007990.1:g.14523_14544delinsAGCAGCGGCGGCGGCGGCAGCT , LRG_674:g.14523_14544delinsAGCAGCGGCGGCGGCGGCAGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000440970.6:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000407914.2:p.Ser158=
ENST00000570206.2:c.181_202delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000456777.2:p.Ser61=
ENST00000685868.1:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000509873.1:p.Ser158=
ENST00000690502.1:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000510560.1:p.Ser158=
ENST00000251020.9:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT MANE Select ENSP00000251020.4:p.Ser158=
ENST00000251020.8:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000251020.4:p.Ser158=
ENST00000440970.5:c.181_202delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000407914.1:p.Ser61=
ENST00000566102.1:c.77-4198_77-4177delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000455582.1:n.77-4198_77-4177delins...
ENST00000570206.1:c.181_202delinsAGCAGCGGCGGCGGCGGCAGCT ENSP00000456777.1:p.Ser61=
NM_001127892.1:c.181_202delinsAGCAGCGGCGGCGGCGGCAGCT NP_001121364.1:p.Ser61=
NM_002968.2:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT , LRG_674t1:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT NP_002959.2:p.Ser158=
XM_006721241.2:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT XP_006721304.1:p.Ser158=
XM_011523254.1:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT XP_011521556.1:p.Ser158=
XM_011523255.1:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT XP_011521557.1:p.Ser158=
NM_002968.3:c.472_493delinsAGCAGCGGCGGCGGCGGCAGCT MANE Select NP_002959.2:p.Ser158=
NM_001127892.2:c.181_202delinsAGCAGCGGCGGCGGCGGCAGCT NP_001121364.1:p.Ser61=