Canonical Allele Identifier: CA395883303

Gene: SALL1

Linked Data

• MyVariant Identifiers: chr16:g.51173227G>A (hg19) ; chr16:g.51139316G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51139316G>A , CM000678.2:g.51139316G>A	GRCh38
NC_000016.9:g.51173227G>A , CM000678.1:g.51173227G>A	GRCh37
NC_000016.8:g.49730728G>A	NCBI36
NG_007990.1:g.16957C>T , LRG_674:g.16957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.2906C>T	ENSP00000407914.2:p.Ala969Val
ENST00000570206.2:c.2615C>T	ENSP00000456777.2:p.Ala872Val
ENST00000685868.1:c.2906C>T	ENSP00000509873.1:p.Ala969Val
ENST00000690502.1:c.2906C>T	ENSP00000510560.1:p.Ala969Val
ENST00000251020.9:c.2906C>T MANE Select	ENSP00000251020.4:p.Ala969Val
ENST00000251020.8:c.2906C>T	ENSP00000251020.4:p.Ala969Val
ENST00000440970.5:c.2615C>T	ENSP00000407914.1:p.Ala872Val
ENST00000566102.1:c.77-1764C>T	ENSP00000455582.1:n.77-1764C>T
ENST00000570206.1:c.2615C>T	ENSP00000456777.1:p.Ala872Val
NM_001127892.1:c.2615C>T	NP_001121364.1:p.Ala872Val
NM_002968.2:c.2906C>T , LRG_674t1:c.2906C>T	NP_002959.2:p.Ala969Val
XM_006721241.2:c.2906C>T	XP_006721304.1:p.Ala969Val
XM_011523254.1:c.2906C>T	XP_011521556.1:p.Ala969Val
XM_011523255.1:c.2906C>T	XP_011521557.1:p.Ala969Val
NM_002968.3:c.2906C>T MANE Select	NP_002959.2:p.Ala969Val
NM_001127892.2:c.2615C>T	NP_001121364.1:p.Ala872Val