Canonical Allele Identifier: CA2816661608

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784818_51784819insAC , CM000682.2:g.51784818_51784819insAC	GRCh38
NC_000020.10:g.50401357_50401358insAC , CM000682.1:g.50401357_50401358insAC	GRCh37
NC_000020.9:g.49834764_49834765insAC	NCBI36
NG_008000.1:g.22691_22692insGT , LRG_675:g.22691_22692insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2743-135_2743-134insGT MANE Select	ENSP00000217086.4:n.2743-135_2743-134insGT
ENST00000217086.8:c.2743-135_2743-134insGT	ENSP00000217086.4:n.2743-135_2743-134insGT
ENST00000371539.7:c.412-135_412-134insGT	ENSP00000360594.3:n.412-135_412-134insGT
ENST00000395997.3:c.1432-135_1432-134insGT	ENSP00000379319.3:n.1432-135_1432-134insGT
NM_020436.3:c.2743-135_2743-134insGT , LRG_675t1:c.2743-135_2743-134insGT	NP_065169.1:n.2743-135_2743-134insGT
XM_005260467.2:c.2437-135_2437-134insGT	XP_005260524.1:n.2437-135_2437-134insGT
XM_006723834.2:c.2437-135_2437-134insGT	XP_006723897.1:n.2437-135_2437-134insGT
XM_011528919.1:c.2617-135_2617-134insGT	XP_011527221.1:n.2617-135_2617-134insGT
XM_011528920.1:c.2437-135_2437-134insGT	XP_011527222.1:n.2437-135_2437-134insGT
XM_011528921.1:c.2437-135_2437-134insGT	XP_011527223.1:n.2437-135_2437-134insGT
XM_011528922.1:c.2437-135_2437-134insGT	XP_011527224.1:n.2437-135_2437-134insGT
XM_011528923.1:c.1432-135_1432-134insGT	XP_011527225.1:n.1432-135_1432-134insGT
NM_001318031.1:c.1432-135_1432-134insGT	NP_001304960.1:n.1432-135_1432-134insGT
NM_020436.4:c.2743-135_2743-134insGT	NP_065169.1:n.2743-135_2743-134insGT
XM_005260467.4:c.2437-135_2437-134insGT	XP_005260524.1:n.2437-135_2437-134insGT
XM_011528921.2:c.2437-135_2437-134insGT	XP_011527223.1:n.2437-135_2437-134insGT
XM_011528922.2:c.2437-135_2437-134insGT	XP_011527224.1:n.2437-135_2437-134insGT
NM_020436.5:c.2743-135_2743-134insGT MANE Select	NP_065169.1:n.2743-135_2743-134insGT
NM_001318031.2:c.1432-135_1432-134insGT	NP_001304960.1:n.1432-135_1432-134insGT