Canonical Allele Identifier: CA2369155266

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784416G= , CM000682.2:g.51784416G=	GRCh38
NC_000020.10:g.50400955G= , CM000682.1:g.50400955G=	GRCh37
NC_000020.9:g.49834362G=	NCBI36
NG_008000.1:g.23094C= , LRG_675:g.23094C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.3011C= MANE Select	ENSP00000217086.4:p.Ala1004=
ENST00000217086.8:c.3011C=	ENSP00000217086.4:p.Ala1004=
ENST00000371539.7:c.680C=	ENSP00000360594.3:p.Ala227=
ENST00000395997.3:c.1700C=	ENSP00000379319.3:p.Ala567=
NM_020436.3:c.3011C= , LRG_675t1:c.3011C=	NP_065169.1:p.Ala1004=
XM_005260467.2:c.2705C=	XP_005260524.1:p.Ala902=
XM_006723834.2:c.2705C=	XP_006723897.1:p.Ala902=
XM_011528919.1:c.2885C=	XP_011527221.1:p.Ala962=
XM_011528920.1:c.2705C=	XP_011527222.1:p.Ala902=
XM_011528921.1:c.2705C=	XP_011527223.1:p.Ala902=
XM_011528922.1:c.2705C=	XP_011527224.1:p.Ala902=
XM_011528923.1:c.1700C=	XP_011527225.1:p.Ala567=
NM_001318031.1:c.1700C=	NP_001304960.1:p.Ala567=
NM_020436.4:c.3011C=	NP_065169.1:p.Ala1004=
XM_005260467.4:c.2705C=	XP_005260524.1:p.Ala902=
XM_011528921.2:c.2705C=	XP_011527223.1:p.Ala902=
XM_011528922.2:c.2705C=	XP_011527224.1:p.Ala902=
NM_020436.5:c.3011C= MANE Select	NP_065169.1:p.Ala1004=
NM_001318031.2:c.1700C=	NP_001304960.1:p.Ala567=