Canonical Allele Identifier: CA2222023117

Gene: SALL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51141786T= , CM000678.2:g.51141786T=	GRCh38
NC_000016.9:g.51175697T= , CM000678.1:g.51175697T=	GRCh37
NC_000016.8:g.49733198T=	NCBI36
NG_007990.1:g.14487A= , LRG_674:g.14487A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440970.6:c.436A=	ENSP00000407914.2:p.Ser146=
ENST00000570206.2:c.145A=	ENSP00000456777.2:p.Ser49=
ENST00000685868.1:c.436A=	ENSP00000509873.1:p.Ser146=
ENST00000690502.1:c.436A=	ENSP00000510560.1:p.Ser146=
ENST00000251020.9:c.436A= MANE Select	ENSP00000251020.4:p.Ser146=
ENST00000251020.8:c.436A=	ENSP00000251020.4:p.Ser146=
ENST00000440970.5:c.145A=	ENSP00000407914.1:p.Ser49=
ENST00000566102.1:c.77-4234A=	ENSP00000455582.1:n.77-4234A=
ENST00000570206.1:c.145A=	ENSP00000456777.1:p.Ser49=
NM_001127892.1:c.145A=	NP_001121364.1:p.Ser49=
NM_002968.2:c.436A= , LRG_674t1:c.436A=	NP_002959.2:p.Ser146=
XM_006721241.2:c.436A=	XP_006721304.1:p.Ser146=
XM_011523254.1:c.436A=	XP_011521556.1:p.Ser146=
XM_011523255.1:c.436A=	XP_011521557.1:p.Ser146=
NM_002968.3:c.436A= MANE Select	NP_002959.2:p.Ser146=
NM_001127892.2:c.145A=	NP_001121364.1:p.Ser49=