Canonical Allele Identifier: CA409006432

Gene: SALL4

Linked Data

• COSMIC: COSM6093935
• MyVariant Identifiers: chr20:g.50405400C>A (hg19) ; chr20:g.51788861C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51788861C>A , CM000682.2:g.51788861C>A	GRCh38
NC_000020.10:g.50405400C>A , CM000682.1:g.50405400C>A	GRCh37
NC_000020.9:g.49838807C>A	NCBI36
NG_008000.1:g.18649G>T , LRG_675:g.18649G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2742G>T MANE Select	ENSP00000217086.4:p.Lys914Asn
ENST00000217086.8:c.2742G>T	ENSP00000217086.4:p.Lys914Asn
ENST00000371539.7:c.411G>T	ENSP00000360594.3:p.Lys137Asn
ENST00000395997.3:c.1431G>T	ENSP00000379319.3:p.Lys477Asn
NM_020436.3:c.2742G>T , LRG_675t1:c.2742G>T	NP_065169.1:p.Lys914Asn
XM_005260467.2:c.2436G>T	XP_005260524.1:p.Lys812Asn
XM_006723834.2:c.2436G>T	XP_006723897.1:p.Lys812Asn
XM_011528919.1:c.2616G>T	XP_011527221.1:p.Lys872Asn
XM_011528920.1:c.2436G>T	XP_011527222.1:p.Lys812Asn
XM_011528921.1:c.2436G>T	XP_011527223.1:p.Lys812Asn
XM_011528922.1:c.2436G>T	XP_011527224.1:p.Lys812Asn
XM_011528923.1:c.1431G>T	XP_011527225.1:p.Lys477Asn
NM_001318031.1:c.1431G>T	NP_001304960.1:p.Lys477Asn
NM_020436.4:c.2742G>T	NP_065169.1:p.Lys914Asn
XM_005260467.4:c.2436G>T	XP_005260524.1:p.Lys812Asn
XM_011528921.2:c.2436G>T	XP_011527223.1:p.Lys812Asn
XM_011528922.2:c.2436G>T	XP_011527224.1:p.Lys812Asn
NM_020436.5:c.2742G>T MANE Select	NP_065169.1:p.Lys914Asn
NM_001318031.2:c.1431G>T	NP_001304960.1:p.Lys477Asn