Canonical Allele Identifier: CA2369155449

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784816G= , CM000682.2:g.51784816G=	GRCh38
NC_000020.10:g.50401355G= , CM000682.1:g.50401355G=	GRCh37
NC_000020.9:g.49834762G=	NCBI36
NG_008000.1:g.22694C= , LRG_675:g.22694C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2743-132C= MANE Select	ENSP00000217086.4:n.2743-132C=
ENST00000217086.8:c.2743-132C=	ENSP00000217086.4:n.2743-132C=
ENST00000371539.7:c.412-132C=	ENSP00000360594.3:n.412-132C=
ENST00000395997.3:c.1432-132C=	ENSP00000379319.3:n.1432-132C=
NM_020436.3:c.2743-132C= , LRG_675t1:c.2743-132C=	NP_065169.1:n.2743-132C=
XM_005260467.2:c.2437-132C=	XP_005260524.1:n.2437-132C=
XM_006723834.2:c.2437-132C=	XP_006723897.1:n.2437-132C=
XM_011528919.1:c.2617-132C=	XP_011527221.1:n.2617-132C=
XM_011528920.1:c.2437-132C=	XP_011527222.1:n.2437-132C=
XM_011528921.1:c.2437-132C=	XP_011527223.1:n.2437-132C=
XM_011528922.1:c.2437-132C=	XP_011527224.1:n.2437-132C=
XM_011528923.1:c.1432-132C=	XP_011527225.1:n.1432-132C=
NM_001318031.1:c.1432-132C=	NP_001304960.1:n.1432-132C=
NM_020436.4:c.2743-132C=	NP_065169.1:n.2743-132C=
XM_005260467.4:c.2437-132C=	XP_005260524.1:n.2437-132C=
XM_011528921.2:c.2437-132C=	XP_011527223.1:n.2437-132C=
XM_011528922.2:c.2437-132C=	XP_011527224.1:n.2437-132C=
NM_020436.5:c.2743-132C= MANE Select	NP_065169.1:n.2743-132C=
NM_001318031.2:c.1432-132C=	NP_001304960.1:n.1432-132C=