Canonical Allele Identifier: CA2816661540
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51784760_51784762del , CM000682.2:g.51784760_51784762del GRCh38
NC_000020.10:g.50401299_50401301del , CM000682.1:g.50401299_50401301del GRCh37
NC_000020.9:g.49834706_49834708del NCBI36
NG_008000.1:g.22748_22750del , LRG_675:g.22748_22750del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217086.9:c.2743-78_2743-76del MANE Select ENSP00000217086.4:n.2743-78_2743-76del
ENST00000217086.8:c.2743-78_2743-76del ENSP00000217086.4:n.2743-78_2743-76del
ENST00000371539.7:c.412-78_412-76del ENSP00000360594.3:n.412-78_412-76del
ENST00000395997.3:c.1432-78_1432-76del ENSP00000379319.3:n.1432-78_1432-76del
NM_020436.3:c.2743-78_2743-76del , LRG_675t1:c.2743-78_2743-76del NP_065169.1:n.2743-78_2743-76del
XM_005260467.2:c.2437-78_2437-76del XP_005260524.1:n.2437-78_2437-76del
XM_006723834.2:c.2437-78_2437-76del XP_006723897.1:n.2437-78_2437-76del
XM_011528919.1:c.2617-78_2617-76del XP_011527221.1:n.2617-78_2617-76del
XM_011528920.1:c.2437-78_2437-76del XP_011527222.1:n.2437-78_2437-76del
XM_011528921.1:c.2437-78_2437-76del XP_011527223.1:n.2437-78_2437-76del
XM_011528922.1:c.2437-78_2437-76del XP_011527224.1:n.2437-78_2437-76del
XM_011528923.1:c.1432-78_1432-76del XP_011527225.1:n.1432-78_1432-76del
NM_001318031.1:c.1432-78_1432-76del NP_001304960.1:n.1432-78_1432-76del
NM_020436.4:c.2743-78_2743-76del NP_065169.1:n.2743-78_2743-76del
XM_005260467.4:c.2437-78_2437-76del XP_005260524.1:n.2437-78_2437-76del
XM_011528921.2:c.2437-78_2437-76del XP_011527223.1:n.2437-78_2437-76del
XM_011528922.2:c.2437-78_2437-76del XP_011527224.1:n.2437-78_2437-76del
NM_020436.5:c.2743-78_2743-76del MANE Select NP_065169.1:n.2743-78_2743-76del
NM_001318031.2:c.1432-78_1432-76del NP_001304960.1:n.1432-78_1432-76del