Canonical Allele Identifier: CA2222022963
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51141746_51141748delinsCTG , CM000678.2:g.51141746_51141748delinsCTG GRCh38
NC_000016.9:g.51175657_51175659delinsCTG , CM000678.1:g.51175657_51175659delinsCTG GRCh37
NC_000016.8:g.49733158_49733160delinsCTG NCBI36
NG_007990.1:g.14525_14527delinsCAG , LRG_674:g.14525_14527delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000440970.6:c.474_476delinsCAG ENSP00000407914.2:p.Ser158=
ENST00000570206.2:c.183_185delinsCAG ENSP00000456777.2:p.Ser61=
ENST00000685868.1:c.474_476delinsCAG ENSP00000509873.1:p.Ser158=
ENST00000690502.1:c.474_476delinsCAG ENSP00000510560.1:p.Ser158=
ENST00000251020.9:c.474_476delinsCAG MANE Select ENSP00000251020.4:p.Ser158=
ENST00000251020.8:c.474_476delinsCAG ENSP00000251020.4:p.Ser158=
ENST00000440970.5:c.183_185delinsCAG ENSP00000407914.1:p.Ser61=
ENST00000566102.1:c.77-4196_77-4194delinsCAG ENSP00000455582.1:n.77-4196_77-4194delins...
ENST00000570206.1:c.183_185delinsCAG ENSP00000456777.1:p.Ser61=
NM_001127892.1:c.183_185delinsCAG NP_001121364.1:p.Ser61=
NM_002968.2:c.474_476delinsCAG , LRG_674t1:c.474_476delinsCAG NP_002959.2:p.Ser158=
XM_006721241.2:c.474_476delinsCAG XP_006721304.1:p.Ser158=
XM_011523254.1:c.474_476delinsCAG XP_011521556.1:p.Ser158=
XM_011523255.1:c.474_476delinsCAG XP_011521557.1:p.Ser158=
NM_002968.3:c.474_476delinsCAG MANE Select NP_002959.2:p.Ser158=
NM_001127892.2:c.183_185delinsCAG NP_001121364.1:p.Ser61=