Canonical Allele Identifier: CA409006032

Gene: SALL4

Linked Data

• MyVariant Identifiers: chr20:g.50401041C>T (hg19) ; chr20:g.51784502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784502C>T , CM000682.2:g.51784502C>T	GRCh38
NC_000020.10:g.50401041C>T , CM000682.1:g.50401041C>T	GRCh37
NC_000020.9:g.49834448C>T	NCBI36
NG_008000.1:g.23008G>A , LRG_675:g.23008G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.2925G>A MANE Select	ENSP00000217086.4:p.Met975Ile
ENST00000217086.8:c.2925G>A	ENSP00000217086.4:p.Met975Ile
ENST00000371539.7:c.594G>A	ENSP00000360594.3:p.Met198Ile
ENST00000395997.3:c.1614G>A	ENSP00000379319.3:p.Met538Ile
NM_020436.3:c.2925G>A , LRG_675t1:c.2925G>A	NP_065169.1:p.Met975Ile
XM_005260467.2:c.2619G>A	XP_005260524.1:p.Met873Ile
XM_006723834.2:c.2619G>A	XP_006723897.1:p.Met873Ile
XM_011528919.1:c.2799G>A	XP_011527221.1:p.Met933Ile
XM_011528920.1:c.2619G>A	XP_011527222.1:p.Met873Ile
XM_011528921.1:c.2619G>A	XP_011527223.1:p.Met873Ile
XM_011528922.1:c.2619G>A	XP_011527224.1:p.Met873Ile
XM_011528923.1:c.1614G>A	XP_011527225.1:p.Met538Ile
NM_001318031.1:c.1614G>A	NP_001304960.1:p.Met538Ile
NM_020436.4:c.2925G>A	NP_065169.1:p.Met975Ile
XM_005260467.4:c.2619G>A	XP_005260524.1:p.Met873Ile
XM_011528921.2:c.2619G>A	XP_011527223.1:p.Met873Ile
XM_011528922.2:c.2619G>A	XP_011527224.1:p.Met873Ile
NM_020436.5:c.2925G>A MANE Select	NP_065169.1:p.Met975Ile
NM_001318031.2:c.1614G>A	NP_001304960.1:p.Met538Ile