Canonical Allele Identifier: CA2816661551
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51784773_51784774insA , CM000682.2:g.51784773_51784774insA GRCh38
NC_000020.10:g.50401312_50401313insA , CM000682.1:g.50401312_50401313insA GRCh37
NC_000020.9:g.49834719_49834720insA NCBI36
NG_008000.1:g.22736_22737insT , LRG_675:g.22736_22737insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000217086.9:c.2743-90_2743-89insT MANE Select ENSP00000217086.4:n.2743-90_2743-89insT
ENST00000217086.8:c.2743-90_2743-89insT ENSP00000217086.4:n.2743-90_2743-89insT
ENST00000371539.7:c.412-90_412-89insT ENSP00000360594.3:n.412-90_412-89insT
ENST00000395997.3:c.1432-90_1432-89insT ENSP00000379319.3:n.1432-90_1432-89insT
NM_020436.3:c.2743-90_2743-89insT , LRG_675t1:c.2743-90_2743-89insT NP_065169.1:n.2743-90_2743-89insT
XM_005260467.2:c.2437-90_2437-89insT XP_005260524.1:n.2437-90_2437-89insT
XM_006723834.2:c.2437-90_2437-89insT XP_006723897.1:n.2437-90_2437-89insT
XM_011528919.1:c.2617-90_2617-89insT XP_011527221.1:n.2617-90_2617-89insT
XM_011528920.1:c.2437-90_2437-89insT XP_011527222.1:n.2437-90_2437-89insT
XM_011528921.1:c.2437-90_2437-89insT XP_011527223.1:n.2437-90_2437-89insT
XM_011528922.1:c.2437-90_2437-89insT XP_011527224.1:n.2437-90_2437-89insT
XM_011528923.1:c.1432-90_1432-89insT XP_011527225.1:n.1432-90_1432-89insT
NM_001318031.1:c.1432-90_1432-89insT NP_001304960.1:n.1432-90_1432-89insT
NM_020436.4:c.2743-90_2743-89insT NP_065169.1:n.2743-90_2743-89insT
XM_005260467.4:c.2437-90_2437-89insT XP_005260524.1:n.2437-90_2437-89insT
XM_011528921.2:c.2437-90_2437-89insT XP_011527223.1:n.2437-90_2437-89insT
XM_011528922.2:c.2437-90_2437-89insT XP_011527224.1:n.2437-90_2437-89insT
NM_020436.5:c.2743-90_2743-89insT MANE Select NP_065169.1:n.2743-90_2743-89insT
NM_001318031.2:c.1432-90_1432-89insT NP_001304960.1:n.1432-90_1432-89insT