Canonical Allele Identifier: CA2816661610
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51784819_51784820insACTT , CM000682.2:g.51784819_51784820insACTT GRCh38
NC_000020.10:g.50401358_50401359insACTT , CM000682.1:g.50401358_50401359insACTT GRCh37
NC_000020.9:g.49834765_49834766insACTT NCBI36
NG_008000.1:g.22690_22691insAAGT , LRG_675:g.22690_22691insAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000217086.9:c.2743-136_2743-135insAAGT MANE Select ENSP00000217086.4:n.2743-136_2743-135insAAGT
ENST00000217086.8:c.2743-136_2743-135insAAGT ENSP00000217086.4:n.2743-136_2743-135insAAGT
ENST00000371539.7:c.412-136_412-135insAAGT ENSP00000360594.3:n.412-136_412-135insAAGT
ENST00000395997.3:c.1432-136_1432-135insAAGT ENSP00000379319.3:n.1432-136_1432-135insAAGT
NM_020436.3:c.2743-136_2743-135insAAGT , LRG_675t1:c.2743-136_2743-135insAAGT NP_065169.1:n.2743-136_2743-135insAAGT
XM_005260467.2:c.2437-136_2437-135insAAGT XP_005260524.1:n.2437-136_2437-135insAAGT
XM_006723834.2:c.2437-136_2437-135insAAGT XP_006723897.1:n.2437-136_2437-135insAAGT
XM_011528919.1:c.2617-136_2617-135insAAGT XP_011527221.1:n.2617-136_2617-135insAAGT
XM_011528920.1:c.2437-136_2437-135insAAGT XP_011527222.1:n.2437-136_2437-135insAAGT
XM_011528921.1:c.2437-136_2437-135insAAGT XP_011527223.1:n.2437-136_2437-135insAAGT
XM_011528922.1:c.2437-136_2437-135insAAGT XP_011527224.1:n.2437-136_2437-135insAAGT
XM_011528923.1:c.1432-136_1432-135insAAGT XP_011527225.1:n.1432-136_1432-135insAAGT
NM_001318031.1:c.1432-136_1432-135insAAGT NP_001304960.1:n.1432-136_1432-135insAAGT
NM_020436.4:c.2743-136_2743-135insAAGT NP_065169.1:n.2743-136_2743-135insAAGT
XM_005260467.4:c.2437-136_2437-135insAAGT XP_005260524.1:n.2437-136_2437-135insAAGT
XM_011528921.2:c.2437-136_2437-135insAAGT XP_011527223.1:n.2437-136_2437-135insAAGT
XM_011528922.2:c.2437-136_2437-135insAAGT XP_011527224.1:n.2437-136_2437-135insAAGT
NM_020436.5:c.2743-136_2743-135insAAGT MANE Select NP_065169.1:n.2743-136_2743-135insAAGT
NM_001318031.2:c.1432-136_1432-135insAAGT NP_001304960.1:n.1432-136_1432-135insAAGT