Canonical Allele Identifier: CA409005725

Gene: SALL4

Linked Data

• MyVariant Identifiers: chr20:g.50400889T>A (hg19) ; chr20:g.51784350T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784350T>A , CM000682.2:g.51784350T>A	GRCh38
NC_000020.10:g.50400889T>A , CM000682.1:g.50400889T>A	GRCh37
NC_000020.9:g.49834296T>A	NCBI36
NG_008000.1:g.23160A>T , LRG_675:g.23160A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.3077A>T MANE Select	ENSP00000217086.4:p.Asp1026Val
ENST00000217086.8:c.3077A>T	ENSP00000217086.4:p.Asp1026Val
ENST00000371539.7:c.746A>T	ENSP00000360594.3:p.Asp249Val
ENST00000395997.3:c.1766A>T	ENSP00000379319.3:p.Asp589Val
NM_020436.3:c.3077A>T , LRG_675t1:c.3077A>T	NP_065169.1:p.Asp1026Val
XM_005260467.2:c.2771A>T	XP_005260524.1:p.Asp924Val
XM_006723834.2:c.2771A>T	XP_006723897.1:p.Asp924Val
XM_011528919.1:c.2951A>T	XP_011527221.1:p.Asp984Val
XM_011528920.1:c.2771A>T	XP_011527222.1:p.Asp924Val
XM_011528921.1:c.2771A>T	XP_011527223.1:p.Asp924Val
XM_011528922.1:c.2771A>T	XP_011527224.1:p.Asp924Val
XM_011528923.1:c.1766A>T	XP_011527225.1:p.Asp589Val
NM_001318031.1:c.1766A>T	NP_001304960.1:p.Asp589Val
NM_020436.4:c.3077A>T	NP_065169.1:p.Asp1026Val
XM_005260467.4:c.2771A>T	XP_005260524.1:p.Asp924Val
XM_011528921.2:c.2771A>T	XP_011527223.1:p.Asp924Val
XM_011528922.2:c.2771A>T	XP_011527224.1:p.Asp924Val
NM_020436.5:c.3077A>T MANE Select	NP_065169.1:p.Asp1026Val
NM_001318031.2:c.1766A>T	NP_001304960.1:p.Asp589Val