Canonical Allele Identifier: CA495781281

Gene: SALL1

Linked Data

• MyVariant Identifiers: chr16:g.51175167A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51141256A>C , CM000678.2:g.51141256A>C	GRCh38
NC_000016.9:g.51175167A>C , CM000678.1:g.51175167A>C	GRCh37
NC_000016.8:g.49732668A>C	NCBI36
NG_007990.1:g.15017T>G , LRG_674:g.15017T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000440970.6:c.966T>G	ENSP00000407914.2:p.Pro322=
ENST00000570206.2:c.675T>G	ENSP00000456777.2:p.Pro225=
ENST00000685868.1:c.966T>G	ENSP00000509873.1:p.Pro322=
ENST00000690502.1:c.966T>G	ENSP00000510560.1:p.Pro322=
ENST00000251020.9:c.966T>G MANE Select	ENSP00000251020.4:p.Pro322=
ENST00000251020.8:c.966T>G	ENSP00000251020.4:p.Pro322=
ENST00000440970.5:c.675T>G	ENSP00000407914.1:p.Pro225=
ENST00000566102.1:c.77-3704T>G	ENSP00000455582.1:n.77-3704T>G
ENST00000570206.1:c.675T>G	ENSP00000456777.1:p.Pro225=
NM_001127892.1:c.675T>G	NP_001121364.1:p.Pro225=
NM_002968.2:c.966T>G , LRG_674t1:c.966T>G	NP_002959.2:p.Pro322=
XM_006721241.2:c.966T>G	XP_006721304.1:p.Pro322=
XM_011523254.1:c.966T>G	XP_011521556.1:p.Pro322=
XM_011523255.1:c.966T>G	XP_011521557.1:p.Pro322=
NM_002968.3:c.966T>G MANE Select	NP_002959.2:p.Pro322=
NM_001127892.2:c.675T>G	NP_001121364.1:p.Pro225=