Canonical Allele Identifier: CA2222077853

Gene: SALL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51136114_51136115delinsTG , CM000678.2:g.51136114_51136115delinsTG	GRCh38
NC_000016.9:g.51170025_51170026delinsTG , CM000678.1:g.51170025_51170026delinsTG	GRCh37
NC_000016.8:g.49727526_49727527delinsTG	NCBI36
NG_007990.1:g.20158_20159delinsCA , LRG_674:g.20158_20159delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.*997_*998delinsCA	ENSP00000407914.2:n.*997_*998delinsCA
ENST00000685868.1:c.*997_*998delinsCA	ENSP00000509873.1:n.*997_*998delinsCA
ENST00000251020.9:c.*997_*998delinsCA MANE Select	ENSP00000251020.4:n.*997_*998delinsCA
ENST00000251020.8:c.*997_*998delinsCA	ENSP00000251020.4:n.*997_*998delinsCA
ENST00000440970.5:c.*997_*998delinsCA	ENSP00000407914.1:n.*997_*998delinsCA
NM_001127892.1:c.*997_*998delinsCA	NP_001121364.1:n.*997_*998delinsCA
NM_002968.2:c.*997_*998delinsCA , LRG_674t1:c.*997_*998delinsCA	NP_002959.2:n.*997_*998delinsCA
XM_006721241.2:c.*997_*998delinsCA	XP_006721304.1:n.*997_*998delinsCA
XM_011523254.1:c.*997_*998delinsCA	XP_011521556.1:n.*997_*998delinsCA
XM_011523255.1:c.*997_*998delinsCA	XP_011521557.1:n.*997_*998delinsCA
NM_002968.3:c.*997_*998delinsCA MANE Select	NP_002959.2:n.*997_*998delinsCA
NM_001127892.2:c.*997_*998delinsCA	NP_001121364.1:n.*997_*998delinsCA