Canonical Allele Identifier: CA395883719
Gene: SALL1 HGNC NCBI

Linked Data

dbSNP Id: rs1597228444

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51139409A>G , CM000678.2:g.51139409A>G GRCh38
NC_000016.9:g.51173320A>G , CM000678.1:g.51173320A>G GRCh37
NC_000016.8:g.49730821A>G NCBI36
NG_007990.1:g.16864T>C , LRG_674:g.16864T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.2813T>C ENSP00000407914.2:p.Phe938Ser
ENST00000570206.2:c.2522T>C ENSP00000456777.2:p.Phe841Ser
ENST00000685868.1:c.2813T>C ENSP00000509873.1:p.Phe938Ser
ENST00000690502.1:c.2813T>C ENSP00000510560.1:p.Phe938Ser
ENST00000251020.9:c.2813T>C MANE Select ENSP00000251020.4:p.Phe938Ser
ENST00000251020.8:c.2813T>C ENSP00000251020.4:p.Phe938Ser
ENST00000440970.5:c.2522T>C ENSP00000407914.1:p.Phe841Ser
ENST00000566102.1:c.77-1857T>C ENSP00000455582.1:n.77-1857T>C
ENST00000570206.1:c.2522T>C ENSP00000456777.1:p.Phe841Ser
NM_001127892.1:c.2522T>C NP_001121364.1:p.Phe841Ser
NM_002968.2:c.2813T>C , LRG_674t1:c.2813T>C NP_002959.2:p.Phe938Ser
XM_006721241.2:c.2813T>C XP_006721304.1:p.Phe938Ser
XM_011523254.1:c.2813T>C XP_011521556.1:p.Phe938Ser
XM_011523255.1:c.2813T>C XP_011521557.1:p.Phe938Ser
NM_002968.3:c.2813T>C MANE Select NP_002959.2:p.Phe938Ser
NM_001127892.2:c.2522T>C NP_001121364.1:p.Phe841Ser