Canonical Allele Identifier: CA395889611

Gene: SALL1

Linked Data

• gnomAD v4: 16-51141131-T-C
• MyVariant Identifiers: chr16:g.51175042T>C (hg19) ; chr16:g.51141131T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51141131T>C , CM000678.2:g.51141131T>C	GRCh38
NC_000016.9:g.51175042T>C , CM000678.1:g.51175042T>C	GRCh37
NC_000016.8:g.49732543T>C	NCBI36
NG_007990.1:g.15142A>G , LRG_674:g.15142A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.1091A>G	ENSP00000407914.2:p.His364Arg
ENST00000570206.2:c.800A>G	ENSP00000456777.2:p.His267Arg
ENST00000685868.1:c.1091A>G	ENSP00000509873.1:p.His364Arg
ENST00000690502.1:c.1091A>G	ENSP00000510560.1:p.His364Arg
ENST00000251020.9:c.1091A>G MANE Select	ENSP00000251020.4:p.His364Arg
ENST00000251020.8:c.1091A>G	ENSP00000251020.4:p.His364Arg
ENST00000440970.5:c.800A>G	ENSP00000407914.1:p.His267Arg
ENST00000566102.1:c.77-3579A>G	ENSP00000455582.1:n.77-3579A>G
ENST00000570206.1:c.800A>G	ENSP00000456777.1:p.His267Arg
NM_001127892.1:c.800A>G	NP_001121364.1:p.His267Arg
NM_002968.2:c.1091A>G , LRG_674t1:c.1091A>G	NP_002959.2:p.His364Arg
XM_006721241.2:c.1091A>G	XP_006721304.1:p.His364Arg
XM_011523254.1:c.1091A>G	XP_011521556.1:p.His364Arg
XM_011523255.1:c.1091A>G	XP_011521557.1:p.His364Arg
NM_002968.3:c.1091A>G MANE Select	NP_002959.2:p.His364Arg
NM_001127892.2:c.800A>G	NP_001121364.1:p.His267Arg