Canonical Allele Identifier: CA2816661602
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51784811_51784812insAGT , CM000682.2:g.51784811_51784812insAGT GRCh38
NC_000020.10:g.50401350_50401351insAGT , CM000682.1:g.50401350_50401351insAGT GRCh37
NC_000020.9:g.49834757_49834758insAGT NCBI36
NG_008000.1:g.22698_22699insACT , LRG_675:g.22698_22699insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000217086.9:c.2743-128_2743-127insACT MANE Select ENSP00000217086.4:n.2743-128_2743-127insACT
ENST00000217086.8:c.2743-128_2743-127insACT ENSP00000217086.4:n.2743-128_2743-127insACT
ENST00000371539.7:c.412-128_412-127insACT ENSP00000360594.3:n.412-128_412-127insACT
ENST00000395997.3:c.1432-128_1432-127insACT ENSP00000379319.3:n.1432-128_1432-127insACT
NM_020436.3:c.2743-128_2743-127insACT , LRG_675t1:c.2743-128_2743-127insACT NP_065169.1:n.2743-128_2743-127insACT
XM_005260467.2:c.2437-128_2437-127insACT XP_005260524.1:n.2437-128_2437-127insACT
XM_006723834.2:c.2437-128_2437-127insACT XP_006723897.1:n.2437-128_2437-127insACT
XM_011528919.1:c.2617-128_2617-127insACT XP_011527221.1:n.2617-128_2617-127insACT
XM_011528920.1:c.2437-128_2437-127insACT XP_011527222.1:n.2437-128_2437-127insACT
XM_011528921.1:c.2437-128_2437-127insACT XP_011527223.1:n.2437-128_2437-127insACT
XM_011528922.1:c.2437-128_2437-127insACT XP_011527224.1:n.2437-128_2437-127insACT
XM_011528923.1:c.1432-128_1432-127insACT XP_011527225.1:n.1432-128_1432-127insACT
NM_001318031.1:c.1432-128_1432-127insACT NP_001304960.1:n.1432-128_1432-127insACT
NM_020436.4:c.2743-128_2743-127insACT NP_065169.1:n.2743-128_2743-127insACT
XM_005260467.4:c.2437-128_2437-127insACT XP_005260524.1:n.2437-128_2437-127insACT
XM_011528921.2:c.2437-128_2437-127insACT XP_011527223.1:n.2437-128_2437-127insACT
XM_011528922.2:c.2437-128_2437-127insACT XP_011527224.1:n.2437-128_2437-127insACT
NM_020436.5:c.2743-128_2743-127insACT MANE Select NP_065169.1:n.2743-128_2743-127insACT
NM_001318031.2:c.1432-128_1432-127insACT NP_001304960.1:n.1432-128_1432-127insACT