Canonical Allele Identifier: CA409008460

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51790529G>C , CM000682.2:g.51790529G>C	GRCh38
NC_000020.10:g.50407068G>C , CM000682.1:g.50407068G>C	GRCh37
NC_000020.9:g.49840475G>C	NCBI36
NG_008000.1:g.16981C>G , LRG_675:g.16981C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020436.5:c.1954C>G MANE Select	NP_065169.1:p.Gln652Glu
ENST00000217086.9:c.1954C>G MANE Select	ENSP00000217086.4:p.Gln652Glu
NM_001318031.1:c.1150+804C>G	NP_001304960.1:n.1150+804C>G
NM_001318031.2:c.1150+804C>G	NP_001304960.1:n.1150+804C>G
NM_020436.3:c.1954C>G , LRG_675t1:c.1954C>G	NP_065169.1:p.Gln652Glu
NM_020436.4:c.1954C>G	NP_065169.1:p.Gln652Glu
ENST00000217086.8:c.1954C>G	ENSP00000217086.4:p.Gln652Glu
ENST00000371539.7:c.131-1388C>G	ENSP00000360594.3:n.131-1388C>G
ENST00000395997.3:c.1150+804C>G	ENSP00000379319.3:n.1150+804C>G
XM_005260467.2:c.1648C>G	XP_005260524.1:p.Gln550Glu
XM_005260467.4:c.1648C>G	XP_005260524.1:p.Gln550Glu
XM_006723834.2:c.1648C>G	XP_006723897.1:p.Gln550Glu
XM_011528919.1:c.1828C>G	XP_011527221.1:p.Gln610Glu
XM_011528920.1:c.1648C>G	XP_011527222.1:p.Gln550Glu
XM_011528921.1:c.1648C>G	XP_011527223.1:p.Gln550Glu
XM_011528921.2:c.1648C>G	XP_011527223.1:p.Gln550Glu
XM_011528922.1:c.1648C>G	XP_011527224.1:p.Gln550Glu
XM_011528922.2:c.1648C>G	XP_011527224.1:p.Gln550Glu
XM_011528923.1:c.1150+804C>G	XP_011527225.1:n.1150+804C>G