Canonical Allele Identifier: CA2369155270

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784430C= , CM000682.2:g.51784430C=	GRCh38
NC_000020.10:g.50400969C= , CM000682.1:g.50400969C=	GRCh37
NC_000020.9:g.49834376C=	NCBI36
NG_008000.1:g.23080G= , LRG_675:g.23080G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2997G= MANE Select	ENSP00000217086.4:p.Pro999=
ENST00000217086.8:c.2997G=	ENSP00000217086.4:p.Pro999=
ENST00000371539.7:c.666G=	ENSP00000360594.3:p.Pro222=
ENST00000395997.3:c.1686G=	ENSP00000379319.3:p.Pro562=
NM_020436.3:c.2997G= , LRG_675t1:c.2997G=	NP_065169.1:p.Pro999=
XM_005260467.2:c.2691G=	XP_005260524.1:p.Pro897=
XM_006723834.2:c.2691G=	XP_006723897.1:p.Pro897=
XM_011528919.1:c.2871G=	XP_011527221.1:p.Pro957=
XM_011528920.1:c.2691G=	XP_011527222.1:p.Pro897=
XM_011528921.1:c.2691G=	XP_011527223.1:p.Pro897=
XM_011528922.1:c.2691G=	XP_011527224.1:p.Pro897=
XM_011528923.1:c.1686G=	XP_011527225.1:p.Pro562=
NM_001318031.1:c.1686G=	NP_001304960.1:p.Pro562=
NM_020436.4:c.2997G=	NP_065169.1:p.Pro999=
XM_005260467.4:c.2691G=	XP_005260524.1:p.Pro897=
XM_011528921.2:c.2691G=	XP_011527223.1:p.Pro897=
XM_011528922.2:c.2691G=	XP_011527224.1:p.Pro897=
NM_020436.5:c.2997G= MANE Select	NP_065169.1:p.Pro999=
NM_001318031.2:c.1686G=	NP_001304960.1:p.Pro562=