Canonical Allele Identifier: CA745390540
Gene: SALL4 HGNC NCBI

Linked Data

dbSNP Id: rs1399860785

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51785009del , CM000682.2:g.51785009del GRCh38
NC_000020.10:g.50401548del , CM000682.1:g.50401548del GRCh37
NC_000020.9:g.49834955del NCBI36
NG_008000.1:g.22503del , LRG_675:g.22503del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217086.9:c.2743-323del MANE Select ENSP00000217086.4:n.2743-323del
ENST00000217086.8:c.2743-323del ENSP00000217086.4:n.2743-323del
ENST00000371539.7:c.412-323del ENSP00000360594.3:n.412-323del
ENST00000395997.3:c.1432-323del ENSP00000379319.3:n.1432-323del
NM_020436.3:c.2743-323del , LRG_675t1:c.2743-323del NP_065169.1:n.2743-323del
XM_005260467.2:c.2437-323del XP_005260524.1:n.2437-323del
XM_006723834.2:c.2437-323del XP_006723897.1:n.2437-323del
XM_011528919.1:c.2617-323del XP_011527221.1:n.2617-323del
XM_011528920.1:c.2437-323del XP_011527222.1:n.2437-323del
XM_011528921.1:c.2437-323del XP_011527223.1:n.2437-323del
XM_011528922.1:c.2437-323del XP_011527224.1:n.2437-323del
XM_011528923.1:c.1432-323del XP_011527225.1:n.1432-323del
NM_001318031.1:c.1432-323del NP_001304960.1:n.1432-323del
NM_020436.4:c.2743-323del NP_065169.1:n.2743-323del
XM_005260467.4:c.2437-323del XP_005260524.1:n.2437-323del
XM_011528921.2:c.2437-323del XP_011527223.1:n.2437-323del
XM_011528922.2:c.2437-323del XP_011527224.1:n.2437-323del
NM_020436.5:c.2743-323del MANE Select NP_065169.1:n.2743-323del
NM_001318031.2:c.1432-323del NP_001304960.1:n.1432-323del