Canonical Allele Identifier: CA2222021294

Gene: SALL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51141061C= , CM000678.2:g.51141061C=	GRCh38
NC_000016.9:g.51174972C= , CM000678.1:g.51174972C=	GRCh37
NC_000016.8:g.49732473C=	NCBI36
NG_007990.1:g.15212G= , LRG_674:g.15212G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000440970.6:c.1161G=	ENSP00000407914.2:p.Ala387=
ENST00000570206.2:c.870G=	ENSP00000456777.2:p.Ala290=
ENST00000685868.1:c.1161G=	ENSP00000509873.1:p.Ala387=
ENST00000690502.1:c.1161G=	ENSP00000510560.1:p.Ala387=
ENST00000251020.9:c.1161G= MANE Select	ENSP00000251020.4:p.Ala387=
ENST00000251020.8:c.1161G=	ENSP00000251020.4:p.Ala387=
ENST00000440970.5:c.870G=	ENSP00000407914.1:p.Ala290=
ENST00000566102.1:c.77-3509G=	ENSP00000455582.1:n.77-3509G=
ENST00000570206.1:c.870G=	ENSP00000456777.1:p.Ala290=
NM_001127892.1:c.870G=	NP_001121364.1:p.Ala290=
NM_002968.2:c.1161G= , LRG_674t1:c.1161G=	NP_002959.2:p.Ala387=
XM_006721241.2:c.1161G=	XP_006721304.1:p.Ala387=
XM_011523254.1:c.1161G=	XP_011521556.1:p.Ala387=
XM_011523255.1:c.1161G=	XP_011521557.1:p.Ala387=
NM_002968.3:c.1161G= MANE Select	NP_002959.2:p.Ala387=
NM_001127892.2:c.870G=	NP_001121364.1:p.Ala290=