Canonical Allele Identifier: CA409006414

Gene: SALL4

Linked Data

• MyVariant Identifiers: chr20:g.50401222A>G (hg19) ; chr20:g.51784683A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784683A>G , CM000682.2:g.51784683A>G	GRCh38
NC_000020.10:g.50401222A>G , CM000682.1:g.50401222A>G	GRCh37
NC_000020.9:g.49834629A>G	NCBI36
NG_008000.1:g.22827T>C , LRG_675:g.22827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2744T>C MANE Select	ENSP00000217086.4:p.Val915Ala
ENST00000217086.8:c.2744T>C	ENSP00000217086.4:p.Val915Ala
ENST00000371539.7:c.413T>C	ENSP00000360594.3:p.Val138Ala
ENST00000395997.3:c.1433T>C	ENSP00000379319.3:p.Val478Ala
NM_020436.3:c.2744T>C , LRG_675t1:c.2744T>C	NP_065169.1:p.Val915Ala
XM_005260467.2:c.2438T>C	XP_005260524.1:p.Val813Ala
XM_006723834.2:c.2438T>C	XP_006723897.1:p.Val813Ala
XM_011528919.1:c.2618T>C	XP_011527221.1:p.Val873Ala
XM_011528920.1:c.2438T>C	XP_011527222.1:p.Val813Ala
XM_011528921.1:c.2438T>C	XP_011527223.1:p.Val813Ala
XM_011528922.1:c.2438T>C	XP_011527224.1:p.Val813Ala
XM_011528923.1:c.1433T>C	XP_011527225.1:p.Val478Ala
NM_001318031.1:c.1433T>C	NP_001304960.1:p.Val478Ala
NM_020436.4:c.2744T>C	NP_065169.1:p.Val915Ala
XM_005260467.4:c.2438T>C	XP_005260524.1:p.Val813Ala
XM_011528921.2:c.2438T>C	XP_011527223.1:p.Val813Ala
XM_011528922.2:c.2438T>C	XP_011527224.1:p.Val813Ala
NM_020436.5:c.2744T>C MANE Select	NP_065169.1:p.Val915Ala
NM_001318031.2:c.1433T>C	NP_001304960.1:p.Val478Ala