Canonical Allele Identifier: CA721411034

Gene: SALL1

Linked Data

• dbSNP Id: rs1389923267
• gnomAD v3: 16-51136239-TTTC-T
• gnomAD v4: 16-51136239-TTTC-T
• MyVariant Identifiers: chr16:g.51170151_51170153del (hg19) ; chr16:g.51136240_51136242del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51136242_51136244del , CM000678.2:g.51136242_51136244del	GRCh38
NC_000016.9:g.51170153_51170155del , CM000678.1:g.51170153_51170155del	GRCh37
NC_000016.8:g.49727654_49727656del	NCBI36
NG_007990.1:g.20031_20033del , LRG_674:g.20031_20033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.*870_*872del	ENSP00000407914.2:n.*870_*872del
ENST00000685868.1:c.*870_*872del	ENSP00000509873.1:n.*870_*872del
ENST00000251020.9:c.*870_*872del MANE Select	ENSP00000251020.4:n.*870_*872del
ENST00000251020.8:c.*870_*872del	ENSP00000251020.4:n.*870_*872del
ENST00000440970.5:c.*870_*872del	ENSP00000407914.1:n.*870_*872del
NM_001127892.1:c.*870_*872del	NP_001121364.1:n.*870_*872del
NM_002968.2:c.*870_*872del , LRG_674t1:c.*870_*872del	NP_002959.2:n.*870_*872del
XM_006721241.2:c.*870_*872del	XP_006721304.1:n.*870_*872del
XM_011523254.1:c.*870_*872del	XP_011521556.1:n.*870_*872del
XM_011523255.1:c.*870_*872del	XP_011521557.1:n.*870_*872del
NM_002968.3:c.*870_*872del MANE Select	NP_002959.2:n.*870_*872del
NM_001127892.2:c.*870_*872del	NP_001121364.1:n.*870_*872del