Canonical Allele Identifier: CA395885458

Gene: SALL1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.51139886A>G , CM000678.2:g.51139886A>G	GRCh38
NC_000016.9:g.51173797A>G , CM000678.1:g.51173797A>G	GRCh37
NC_000016.8:g.49731298A>G	NCBI36
NG_007990.1:g.16387T>C , LRG_674:g.16387T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002968.3:c.2336T>C MANE Select	NP_002959.2:p.Val779Ala
ENST00000251020.9:c.2336T>C MANE Select	ENSP00000251020.4:p.Val779Ala
NM_001127892.1:c.2045T>C	NP_001121364.1:p.Val682Ala
NM_001127892.2:c.2045T>C	NP_001121364.1:p.Val682Ala
NM_002968.2:c.2336T>C , LRG_674t1:c.2336T>C	NP_002959.2:p.Val779Ala
ENST00000251020.8:c.2336T>C	ENSP00000251020.4:p.Val779Ala
ENST00000440970.5:c.2045T>C	ENSP00000407914.1:p.Val682Ala
ENST00000440970.6:c.2336T>C	ENSP00000407914.2:p.Val779Ala
ENST00000566102.1:c.77-2334T>C	ENSP00000455582.1:n.77-2334T>C
ENST00000570206.1:c.2045T>C	ENSP00000456777.1:p.Val682Ala
ENST00000570206.2:c.2045T>C	ENSP00000456777.2:p.Val682Ala
ENST00000685868.1:c.2336T>C	ENSP00000509873.1:p.Val779Ala
ENST00000690502.1:c.2336T>C	ENSP00000510560.1:p.Val779Ala
XM_006721241.2:c.2336T>C	XP_006721304.1:p.Val779Ala
XM_011523254.1:c.2336T>C	XP_011521556.1:p.Val779Ala
XM_011523255.1:c.2336T>C	XP_011521557.1:p.Val779Ala