Canonical Allele Identifier: CA395890235

Gene: SALL1

Linked Data

• MyVariant Identifiers: chr16:g.51175171A>T (hg19) ; chr16:g.51141260A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51141260A>T , CM000678.2:g.51141260A>T	GRCh38
NC_000016.9:g.51175171A>T , CM000678.1:g.51175171A>T	GRCh37
NC_000016.8:g.49732672A>T	NCBI36
NG_007990.1:g.15013T>A , LRG_674:g.15013T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000440970.6:c.962T>A	ENSP00000407914.2:p.Leu321Gln
ENST00000570206.2:c.671T>A	ENSP00000456777.2:p.Leu224Gln
ENST00000685868.1:c.962T>A	ENSP00000509873.1:p.Leu321Gln
ENST00000690502.1:c.962T>A	ENSP00000510560.1:p.Leu321Gln
ENST00000251020.9:c.962T>A MANE Select	ENSP00000251020.4:p.Leu321Gln
ENST00000251020.8:c.962T>A	ENSP00000251020.4:p.Leu321Gln
ENST00000440970.5:c.671T>A	ENSP00000407914.1:p.Leu224Gln
ENST00000566102.1:c.77-3708T>A	ENSP00000455582.1:n.77-3708T>A
ENST00000570206.1:c.671T>A	ENSP00000456777.1:p.Leu224Gln
NM_001127892.1:c.671T>A	NP_001121364.1:p.Leu224Gln
NM_002968.2:c.962T>A , LRG_674t1:c.962T>A	NP_002959.2:p.Leu321Gln
XM_006721241.2:c.962T>A	XP_006721304.1:p.Leu321Gln
XM_011523254.1:c.962T>A	XP_011521556.1:p.Leu321Gln
XM_011523255.1:c.962T>A	XP_011521557.1:p.Leu321Gln
NM_002968.3:c.962T>A MANE Select	NP_002959.2:p.Leu321Gln
NM_001127892.2:c.671T>A	NP_001121364.1:p.Leu224Gln