Canonical Allele Identifier: CA511025567

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51789101C>T , CM000682.2:g.51789101C>T	GRCh38
NC_000020.10:g.50405640C>T , CM000682.1:g.50405640C>T	GRCh37
NC_000020.9:g.49839047C>T	NCBI36
NG_008000.1:g.18409G>A , LRG_675:g.18409G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020436.5:c.2502G>A MANE Select	NP_065169.1:p.Pro834=
ENST00000217086.9:c.2502G>A MANE Select	ENSP00000217086.4:p.Pro834=
NM_001318031.1:c.1191G>A	NP_001304960.1:p.Pro397=
NM_001318031.2:c.1191G>A	NP_001304960.1:p.Pro397=
NM_020436.3:c.2502G>A , LRG_675t1:c.2502G>A	NP_065169.1:p.Pro834=
NM_020436.4:c.2502G>A	NP_065169.1:p.Pro834=
ENST00000217086.8:c.2502G>A	ENSP00000217086.4:p.Pro834=
ENST00000371539.7:c.171G>A	ENSP00000360594.3:p.Pro57=
ENST00000395997.3:c.1191G>A	ENSP00000379319.3:p.Pro397=
XM_005260467.2:c.2196G>A	XP_005260524.1:p.Pro732=
XM_005260467.4:c.2196G>A	XP_005260524.1:p.Pro732=
XM_006723834.2:c.2196G>A	XP_006723897.1:p.Pro732=
XM_011528919.1:c.2376G>A	XP_011527221.1:p.Pro792=
XM_011528920.1:c.2196G>A	XP_011527222.1:p.Pro732=
XM_011528921.1:c.2196G>A	XP_011527223.1:p.Pro732=
XM_011528921.2:c.2196G>A	XP_011527223.1:p.Pro732=
XM_011528922.1:c.2196G>A	XP_011527224.1:p.Pro732=
XM_011528922.2:c.2196G>A	XP_011527224.1:p.Pro732=
XM_011528923.1:c.1191G>A	XP_011527225.1:p.Pro397=