Canonical Allele Identifier: CA2369155147
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51784181_51784184delinsCAGG , CM000682.2:g.51784181_51784184delinsCAGG GRCh38
NC_000020.10:g.50400720_50400723delinsCAGG , CM000682.1:g.50400720_50400723delinsCAGG GRCh37
NC_000020.9:g.49834127_49834130delinsCAGG NCBI36
NG_008000.1:g.23326_23329delinsCCTG , LRG_675:g.23326_23329delinsCCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000217086.9:c.*81_*84delinsCCTG MANE Select ENSP00000217086.4:n.*81_*84delinsCCTG
ENST00000217086.8:c.*81_*84delinsCCTG ENSP00000217086.4:n.*81_*84delinsCCTG
ENST00000371539.7:c.*81_*84delinsCCTG ENSP00000360594.3:n.*81_*84delinsCCTG
NM_020436.3:c.*81_*84delinsCCTG , LRG_675t1:c.*81_*84delinsCCTG NP_065169.1:n.*81_*84delinsCCTG
XM_005260467.2:c.*81_*84delinsCCTG XP_005260524.1:n.*81_*84delinsCCTG
XM_006723834.2:c.*81_*84delinsCCTG XP_006723897.1:n.*81_*84delinsCCTG
XM_011528919.1:c.*81_*84delinsCCTG XP_011527221.1:n.*81_*84delinsCCTG
XM_011528920.1:c.*81_*84delinsCCTG XP_011527222.1:n.*81_*84delinsCCTG
XM_011528921.1:c.*81_*84delinsCCTG XP_011527223.1:n.*81_*84delinsCCTG
XM_011528922.1:c.*81_*84delinsCCTG XP_011527224.1:n.*81_*84delinsCCTG
XM_011528923.1:c.*81_*84delinsCCTG XP_011527225.1:n.*81_*84delinsCCTG
NM_001318031.1:c.*81_*84delinsCCTG NP_001304960.1:n.*81_*84delinsCCTG
NM_020436.4:c.*81_*84delinsCCTG NP_065169.1:n.*81_*84delinsCCTG
XM_005260467.4:c.*81_*84delinsCCTG XP_005260524.1:n.*81_*84delinsCCTG
XM_011528921.2:c.*81_*84delinsCCTG XP_011527223.1:n.*81_*84delinsCCTG
XM_011528922.2:c.*81_*84delinsCCTG XP_011527224.1:n.*81_*84delinsCCTG
NM_020436.5:c.*81_*84delinsCCTG MANE Select NP_065169.1:n.*81_*84delinsCCTG
NM_001318031.2:c.*81_*84delinsCCTG NP_001304960.1:n.*81_*84delinsCCTG