Canonical Allele Identifier: CA2369155145

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784167_51784170delinsTAAG , CM000682.2:g.51784167_51784170delinsTAAG	GRCh38
NC_000020.10:g.50400706_50400709delinsTAAG , CM000682.1:g.50400706_50400709delinsTAAG	GRCh37
NC_000020.9:g.49834113_49834116delinsTAAG	NCBI36
NG_008000.1:g.23340_23343delinsCTTA , LRG_675:g.23340_23343delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.*95_*98delinsCTTA MANE Select	ENSP00000217086.4:n.*95_*98delinsCTTA
ENST00000217086.8:c.*95_*98delinsCTTA	ENSP00000217086.4:n.*95_*98delinsCTTA
ENST00000371539.7:c.*95_*98delinsCTTA	ENSP00000360594.3:n.*95_*98delinsCTTA
NM_020436.3:c.*95_*98delinsCTTA , LRG_675t1:c.*95_*98delinsCTTA	NP_065169.1:n.*95_*98delinsCTTA
XM_005260467.2:c.*95_*98delinsCTTA	XP_005260524.1:n.*95_*98delinsCTTA
XM_006723834.2:c.*95_*98delinsCTTA	XP_006723897.1:n.*95_*98delinsCTTA
XM_011528919.1:c.*95_*98delinsCTTA	XP_011527221.1:n.*95_*98delinsCTTA
XM_011528920.1:c.*95_*98delinsCTTA	XP_011527222.1:n.*95_*98delinsCTTA
XM_011528921.1:c.*95_*98delinsCTTA	XP_011527223.1:n.*95_*98delinsCTTA
XM_011528922.1:c.*95_*98delinsCTTA	XP_011527224.1:n.*95_*98delinsCTTA
XM_011528923.1:c.*95_*98delinsCTTA	XP_011527225.1:n.*95_*98delinsCTTA
NM_001318031.1:c.*95_*98delinsCTTA	NP_001304960.1:n.*95_*98delinsCTTA
NM_020436.4:c.*95_*98delinsCTTA	NP_065169.1:n.*95_*98delinsCTTA
XM_005260467.4:c.*95_*98delinsCTTA	XP_005260524.1:n.*95_*98delinsCTTA
XM_011528921.2:c.*95_*98delinsCTTA	XP_011527223.1:n.*95_*98delinsCTTA
XM_011528922.2:c.*95_*98delinsCTTA	XP_011527224.1:n.*95_*98delinsCTTA
NM_020436.5:c.*95_*98delinsCTTA MANE Select	NP_065169.1:n.*95_*98delinsCTTA
NM_001318031.2:c.*95_*98delinsCTTA	NP_001304960.1:n.*95_*98delinsCTTA