Canonical Allele Identifier: CA2222017393
Gene: SALL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51139081G= , CM000678.2:g.51139081G= GRCh38
NC_000016.9:g.51172992G= , CM000678.1:g.51172992G= GRCh37
NC_000016.8:g.49730493G= NCBI36
NG_007990.1:g.17192C= , LRG_674:g.17192C=

Transcript Alleles

HGVS Amino-acid change
ENST00000440970.6:c.3141C= ENSP00000407914.2:p.His1047=
ENST00000570206.2:c.2850C= ENSP00000456777.2:p.His950=
ENST00000685868.1:c.3141C= ENSP00000509873.1:p.His1047=
ENST00000690502.1:c.3141C= ENSP00000510560.1:p.His1047=
ENST00000251020.9:c.3141C= MANE Select ENSP00000251020.4:p.His1047=
ENST00000251020.8:c.3141C= ENSP00000251020.4:p.His1047=
ENST00000440970.5:c.2850C= ENSP00000407914.1:p.His950=
ENST00000566102.1:c.77-1529C= ENSP00000455582.1:n.77-1529C=
ENST00000570206.1:c.2850C= ENSP00000456777.1:p.His950=
NM_001127892.1:c.2850C= NP_001121364.1:p.His950=
NM_002968.2:c.3141C= , LRG_674t1:c.3141C= NP_002959.2:p.His1047=
XM_006721241.2:c.3141C= XP_006721304.1:p.His1047=
XM_011523254.1:c.3141C= XP_011521556.1:p.His1047=
XM_011523255.1:c.3141C= XP_011521557.1:p.His1047=
NM_002968.3:c.3141C= MANE Select NP_002959.2:p.His1047=
NM_001127892.2:c.2850C= NP_001121364.1:p.His950=