Canonical Allele Identifier: CA409006227

Gene: SALL4

Linked Data

• dbSNP Id: rs143702441
• gnomAD v4: 20-51784592-G-T
• MyVariant Identifiers: chr20:g.50401131G>T (hg19) ; chr20:g.51784592G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784592G>T , CM000682.2:g.51784592G>T	GRCh38
NC_000020.10:g.50401131G>T , CM000682.1:g.50401131G>T	GRCh37
NC_000020.9:g.49834538G>T	NCBI36
NG_008000.1:g.22918C>A , LRG_675:g.22918C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.2835C>A MANE Select	ENSP00000217086.4:p.Asp945Glu
ENST00000217086.8:c.2835C>A	ENSP00000217086.4:p.Asp945Glu
ENST00000371539.7:c.504C>A	ENSP00000360594.3:p.Asp168Glu
ENST00000395997.3:c.1524C>A	ENSP00000379319.3:p.Asp508Glu
NM_020436.3:c.2835C>A , LRG_675t1:c.2835C>A	NP_065169.1:p.Asp945Glu
XM_005260467.2:c.2529C>A	XP_005260524.1:p.Asp843Glu
XM_006723834.2:c.2529C>A	XP_006723897.1:p.Asp843Glu
XM_011528919.1:c.2709C>A	XP_011527221.1:p.Asp903Glu
XM_011528920.1:c.2529C>A	XP_011527222.1:p.Asp843Glu
XM_011528921.1:c.2529C>A	XP_011527223.1:p.Asp843Glu
XM_011528922.1:c.2529C>A	XP_011527224.1:p.Asp843Glu
XM_011528923.1:c.1524C>A	XP_011527225.1:p.Asp508Glu
NM_001318031.1:c.1524C>A	NP_001304960.1:p.Asp508Glu
NM_020436.4:c.2835C>A	NP_065169.1:p.Asp945Glu
XM_005260467.4:c.2529C>A	XP_005260524.1:p.Asp843Glu
XM_011528921.2:c.2529C>A	XP_011527223.1:p.Asp843Glu
XM_011528922.2:c.2529C>A	XP_011527224.1:p.Asp843Glu
NM_020436.5:c.2835C>A MANE Select	NP_065169.1:p.Asp945Glu
NM_001318031.2:c.1524C>A	NP_001304960.1:p.Asp508Glu