Canonical Allele Identifier: CA409005947

Gene: SALL4

Linked Data

• MyVariant Identifiers: chr20:g.50401000A>T (hg19) ; chr20:g.51784461A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784461A>T , CM000682.2:g.51784461A>T	GRCh38
NC_000020.10:g.50401000A>T , CM000682.1:g.50401000A>T	GRCh37
NC_000020.9:g.49834407A>T	NCBI36
NG_008000.1:g.23049T>A , LRG_675:g.23049T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.2966T>A MANE Select	ENSP00000217086.4:p.Val989Glu
ENST00000217086.8:c.2966T>A	ENSP00000217086.4:p.Val989Glu
ENST00000371539.7:c.635T>A	ENSP00000360594.3:p.Val212Glu
ENST00000395997.3:c.1655T>A	ENSP00000379319.3:p.Val552Glu
NM_020436.3:c.2966T>A , LRG_675t1:c.2966T>A	NP_065169.1:p.Val989Glu
XM_005260467.2:c.2660T>A	XP_005260524.1:p.Val887Glu
XM_006723834.2:c.2660T>A	XP_006723897.1:p.Val887Glu
XM_011528919.1:c.2840T>A	XP_011527221.1:p.Val947Glu
XM_011528920.1:c.2660T>A	XP_011527222.1:p.Val887Glu
XM_011528921.1:c.2660T>A	XP_011527223.1:p.Val887Glu
XM_011528922.1:c.2660T>A	XP_011527224.1:p.Val887Glu
XM_011528923.1:c.1655T>A	XP_011527225.1:p.Val552Glu
NM_001318031.1:c.1655T>A	NP_001304960.1:p.Val552Glu
NM_020436.4:c.2966T>A	NP_065169.1:p.Val989Glu
XM_005260467.4:c.2660T>A	XP_005260524.1:p.Val887Glu
XM_011528921.2:c.2660T>A	XP_011527223.1:p.Val887Glu
XM_011528922.2:c.2660T>A	XP_011527224.1:p.Val887Glu
NM_020436.5:c.2966T>A MANE Select	NP_065169.1:p.Val989Glu
NM_001318031.2:c.1655T>A	NP_001304960.1:p.Val552Glu