Canonical Allele Identifier: CA511025676

Gene: SALL4

Linked Data

• MyVariant Identifiers: chr20:g.50405409G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51788870G>A , CM000682.2:g.51788870G>A	GRCh38
NC_000020.10:g.50405409G>A , CM000682.1:g.50405409G>A	GRCh37
NC_000020.9:g.49838816G>A	NCBI36
NG_008000.1:g.18640C>T , LRG_675:g.18640C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.2733C>T MANE Select	ENSP00000217086.4:p.Gly911=
ENST00000217086.8:c.2733C>T	ENSP00000217086.4:p.Gly911=
ENST00000371539.7:c.402C>T	ENSP00000360594.3:p.Gly134=
ENST00000395997.3:c.1422C>T	ENSP00000379319.3:p.Gly474=
NM_020436.3:c.2733C>T , LRG_675t1:c.2733C>T	NP_065169.1:p.Gly911=
XM_005260467.2:c.2427C>T	XP_005260524.1:p.Gly809=
XM_006723834.2:c.2427C>T	XP_006723897.1:p.Gly809=
XM_011528919.1:c.2607C>T	XP_011527221.1:p.Gly869=
XM_011528920.1:c.2427C>T	XP_011527222.1:p.Gly809=
XM_011528921.1:c.2427C>T	XP_011527223.1:p.Gly809=
XM_011528922.1:c.2427C>T	XP_011527224.1:p.Gly809=
XM_011528923.1:c.1422C>T	XP_011527225.1:p.Gly474=
NM_001318031.1:c.1422C>T	NP_001304960.1:p.Gly474=
NM_020436.4:c.2733C>T	NP_065169.1:p.Gly911=
XM_005260467.4:c.2427C>T	XP_005260524.1:p.Gly809=
XM_011528921.2:c.2427C>T	XP_011527223.1:p.Gly809=
XM_011528922.2:c.2427C>T	XP_011527224.1:p.Gly809=
NM_020436.5:c.2733C>T MANE Select	NP_065169.1:p.Gly911=
NM_001318031.2:c.1422C>T	NP_001304960.1:p.Gly474=