Canonical Allele Identifier: CA658115409

Gene: SALL4

Linked Data

• COSMIC: COSN20093784

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784179_51784180insC , CM000682.2:g.51784179_51784180insC	GRCh38
NC_000020.10:g.50400718_50400719insC , CM000682.1:g.50400718_50400719insC	GRCh37
NC_000020.9:g.49834125_49834126insC	NCBI36
NG_008000.1:g.23330_23331insG , LRG_675:g.23330_23331insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.*85_*86insG MANE Select	ENSP00000217086.4:n.*85_*86insG
ENST00000217086.8:c.*85_*86insG	ENSP00000217086.4:n.*85_*86insG
ENST00000371539.7:c.*85_*86insG	ENSP00000360594.3:n.*85_*86insG
NM_020436.3:c.*85_*86insG , LRG_675t1:c.*85_*86insG	NP_065169.1:n.*85_*86insG
XM_005260467.2:c.*85_*86insG	XP_005260524.1:n.*85_*86insG
XM_006723834.2:c.*85_*86insG	XP_006723897.1:n.*85_*86insG
XM_011528919.1:c.*85_*86insG	XP_011527221.1:n.*85_*86insG
XM_011528920.1:c.*85_*86insG	XP_011527222.1:n.*85_*86insG
XM_011528921.1:c.*85_*86insG	XP_011527223.1:n.*85_*86insG
XM_011528922.1:c.*85_*86insG	XP_011527224.1:n.*85_*86insG
XM_011528923.1:c.*85_*86insG	XP_011527225.1:n.*85_*86insG
NM_001318031.1:c.*85_*86insG	NP_001304960.1:n.*85_*86insG
NM_020436.4:c.*85_*86insG	NP_065169.1:n.*85_*86insG
XM_005260467.4:c.*85_*86insG	XP_005260524.1:n.*85_*86insG
XM_011528921.2:c.*85_*86insG	XP_011527223.1:n.*85_*86insG
XM_011528922.2:c.*85_*86insG	XP_011527224.1:n.*85_*86insG
NM_020436.5:c.*85_*86insG MANE Select	NP_065169.1:n.*85_*86insG
NM_001318031.2:c.*85_*86insG	NP_001304960.1:n.*85_*86insG