Canonical Allele Identifier: CA2222078105
Gene: SALL1 HGNC NCBI

Linked Data

dbSNP Id: rs1962296141

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51136282_51136283insCAACTGAA , CM000678.2:g.51136282_51136283insCAACTGAA GRCh38
NC_000016.9:g.51170193_51170194insCAACTGAA , CM000678.1:g.51170193_51170194insCAACTGAA GRCh37
NC_000016.8:g.49727694_49727695insCAACTGAA NCBI36
NG_007990.1:g.19996_19997insTGTTCAGT , LRG_674:g.19996_19997insTGTTCAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.*835_*836insTGTTCAGT ENSP00000407914.2:n.*835_*836insTGTTCAGT
ENST00000685868.1:c.*835_*836insTGTTCAGT ENSP00000509873.1:n.*835_*836insTGTTCAGT
ENST00000251020.9:c.*835_*836insTGTTCAGT MANE Select ENSP00000251020.4:n.*835_*836insTGTTCAGT
ENST00000251020.8:c.*835_*836insTGTTCAGT ENSP00000251020.4:n.*835_*836insTGTTCAGT
ENST00000440970.5:c.*835_*836insTGTTCAGT ENSP00000407914.1:n.*835_*836insTGTTCAGT
NM_001127892.1:c.*835_*836insTGTTCAGT NP_001121364.1:n.*835_*836insTGTTCAGT
NM_002968.2:c.*835_*836insTGTTCAGT , LRG_674t1:c.*835_*836insTGTTCAGT NP_002959.2:n.*835_*836insTGTTCAGT
XM_006721241.2:c.*835_*836insTGTTCAGT XP_006721304.1:n.*835_*836insTGTTCAGT
XM_011523254.1:c.*835_*836insTGTTCAGT XP_011521556.1:n.*835_*836insTGTTCAGT
XM_011523255.1:c.*835_*836insTGTTCAGT XP_011521557.1:n.*835_*836insTGTTCAGT
NM_002968.3:c.*835_*836insTGTTCAGT MANE Select NP_002959.2:n.*835_*836insTGTTCAGT
NM_001127892.2:c.*835_*836insTGTTCAGT NP_001121364.1:n.*835_*836insTGTTCAGT