Canonical Allele Identifier: CA745389516

Gene: SALL4

Linked Data

• dbSNP Id: rs1394880416
• gnomAD v4: 20-51784167-TAAG-T
• MyVariant Identifiers: chr20:g.50400707_50400709del (hg19) ; chr20:g.51784168_51784170del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784170_51784172del , CM000682.2:g.51784170_51784172del	GRCh38
NC_000020.10:g.50400709_50400711del , CM000682.1:g.50400709_50400711del	GRCh37
NC_000020.9:g.49834116_49834118del	NCBI36
NG_008000.1:g.23340_23342del , LRG_675:g.23340_23342del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.*95_*97del MANE Select	ENSP00000217086.4:n.*95_*97del
ENST00000217086.8:c.*95_*97del	ENSP00000217086.4:n.*95_*97del
ENST00000371539.7:c.*95_*97del	ENSP00000360594.3:n.*95_*97del
NM_020436.3:c.*95_*97del , LRG_675t1:c.*95_*97del	NP_065169.1:n.*95_*97del
XM_005260467.2:c.*95_*97del	XP_005260524.1:n.*95_*97del
XM_006723834.2:c.*95_*97del	XP_006723897.1:n.*95_*97del
XM_011528919.1:c.*95_*97del	XP_011527221.1:n.*95_*97del
XM_011528920.1:c.*95_*97del	XP_011527222.1:n.*95_*97del
XM_011528921.1:c.*95_*97del	XP_011527223.1:n.*95_*97del
XM_011528922.1:c.*95_*97del	XP_011527224.1:n.*95_*97del
XM_011528923.1:c.*95_*97del	XP_011527225.1:n.*95_*97del
NM_001318031.1:c.*95_*97del	NP_001304960.1:n.*95_*97del
NM_020436.4:c.*95_*97del	NP_065169.1:n.*95_*97del
XM_005260467.4:c.*95_*97del	XP_005260524.1:n.*95_*97del
XM_011528921.2:c.*95_*97del	XP_011527223.1:n.*95_*97del
XM_011528922.2:c.*95_*97del	XP_011527224.1:n.*95_*97del
NM_020436.5:c.*95_*97del MANE Select	NP_065169.1:n.*95_*97del
NM_001318031.2:c.*95_*97del	NP_001304960.1:n.*95_*97del