Canonical Allele Identifier: CA395882544
Gene: SALL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.51139209T>C , CM000678.2:g.51139209T>C GRCh38
NC_000016.9:g.51173120T>C , CM000678.1:g.51173120T>C GRCh37
NC_000016.8:g.49730621T>C NCBI36
NG_007990.1:g.17064A>G , LRG_674:g.17064A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000440970.6:c.3013A>G ENSP00000407914.2:p.Ile1005Val
ENST00000570206.2:c.2722A>G ENSP00000456777.2:p.Ile908Val
ENST00000685868.1:c.3013A>G ENSP00000509873.1:p.Ile1005Val
ENST00000690502.1:c.3013A>G ENSP00000510560.1:p.Ile1005Val
ENST00000251020.9:c.3013A>G MANE Select ENSP00000251020.4:p.Ile1005Val
ENST00000251020.8:c.3013A>G ENSP00000251020.4:p.Ile1005Val
ENST00000440970.5:c.2722A>G ENSP00000407914.1:p.Ile908Val
ENST00000566102.1:c.77-1657A>G ENSP00000455582.1:n.77-1657A>G
ENST00000570206.1:c.2722A>G ENSP00000456777.1:p.Ile908Val
NM_001127892.1:c.2722A>G NP_001121364.1:p.Ile908Val
NM_002968.2:c.3013A>G , LRG_674t1:c.3013A>G NP_002959.2:p.Ile1005Val
XM_006721241.2:c.3013A>G XP_006721304.1:p.Ile1005Val
XM_011523254.1:c.3013A>G XP_011521556.1:p.Ile1005Val
XM_011523255.1:c.3013A>G XP_011521557.1:p.Ile1005Val
NM_002968.3:c.3013A>G MANE Select NP_002959.2:p.Ile1005Val
NM_001127892.2:c.2722A>G NP_001121364.1:p.Ile908Val