Canonical Allele Identifier: CA2816661515
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51784726_51784728del , CM000682.2:g.51784726_51784728del GRCh38
NC_000020.10:g.50401265_50401267del , CM000682.1:g.50401265_50401267del GRCh37
NC_000020.9:g.49834672_49834674del NCBI36
NG_008000.1:g.22782_22784del , LRG_675:g.22782_22784del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217086.9:c.2743-44_2743-42del MANE Select ENSP00000217086.4:n.2743-44_2743-42del
ENST00000217086.8:c.2743-44_2743-42del ENSP00000217086.4:n.2743-44_2743-42del
ENST00000371539.7:c.412-44_412-42del ENSP00000360594.3:n.412-44_412-42del
ENST00000395997.3:c.1432-44_1432-42del ENSP00000379319.3:n.1432-44_1432-42del
NM_020436.3:c.2743-44_2743-42del , LRG_675t1:c.2743-44_2743-42del NP_065169.1:n.2743-44_2743-42del
XM_005260467.2:c.2437-44_2437-42del XP_005260524.1:n.2437-44_2437-42del
XM_006723834.2:c.2437-44_2437-42del XP_006723897.1:n.2437-44_2437-42del
XM_011528919.1:c.2617-44_2617-42del XP_011527221.1:n.2617-44_2617-42del
XM_011528920.1:c.2437-44_2437-42del XP_011527222.1:n.2437-44_2437-42del
XM_011528921.1:c.2437-44_2437-42del XP_011527223.1:n.2437-44_2437-42del
XM_011528922.1:c.2437-44_2437-42del XP_011527224.1:n.2437-44_2437-42del
XM_011528923.1:c.1432-44_1432-42del XP_011527225.1:n.1432-44_1432-42del
NM_001318031.1:c.1432-44_1432-42del NP_001304960.1:n.1432-44_1432-42del
NM_020436.4:c.2743-44_2743-42del NP_065169.1:n.2743-44_2743-42del
XM_005260467.4:c.2437-44_2437-42del XP_005260524.1:n.2437-44_2437-42del
XM_011528921.2:c.2437-44_2437-42del XP_011527223.1:n.2437-44_2437-42del
XM_011528922.2:c.2437-44_2437-42del XP_011527224.1:n.2437-44_2437-42del
NM_020436.5:c.2743-44_2743-42del MANE Select NP_065169.1:n.2743-44_2743-42del
NM_001318031.2:c.1432-44_1432-42del NP_001304960.1:n.1432-44_1432-42del