Canonical Allele Identifier: CA511025696

Gene: SALL4

Linked Data

• gnomAD v4: 20-51784394-G-A
• MyVariant Identifiers: chr20:g.50400933G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784394G>A , CM000682.2:g.51784394G>A	GRCh38
NC_000020.10:g.50400933G>A , CM000682.1:g.50400933G>A	GRCh37
NC_000020.9:g.49834340G>A	NCBI36
NG_008000.1:g.23116C>T , LRG_675:g.23116C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.3033C>T MANE Select	ENSP00000217086.4:p.Ala1011=
ENST00000217086.8:c.3033C>T	ENSP00000217086.4:p.Ala1011=
ENST00000371539.7:c.702C>T	ENSP00000360594.3:p.Ala234=
ENST00000395997.3:c.1722C>T	ENSP00000379319.3:p.Ala574=
NM_020436.3:c.3033C>T , LRG_675t1:c.3033C>T	NP_065169.1:p.Ala1011=
XM_005260467.2:c.2727C>T	XP_005260524.1:p.Ala909=
XM_006723834.2:c.2727C>T	XP_006723897.1:p.Ala909=
XM_011528919.1:c.2907C>T	XP_011527221.1:p.Ala969=
XM_011528920.1:c.2727C>T	XP_011527222.1:p.Ala909=
XM_011528921.1:c.2727C>T	XP_011527223.1:p.Ala909=
XM_011528922.1:c.2727C>T	XP_011527224.1:p.Ala909=
XM_011528923.1:c.1722C>T	XP_011527225.1:p.Ala574=
NM_001318031.1:c.1722C>T	NP_001304960.1:p.Ala574=
NM_020436.4:c.3033C>T	NP_065169.1:p.Ala1011=
XM_005260467.4:c.2727C>T	XP_005260524.1:p.Ala909=
XM_011528921.2:c.2727C>T	XP_011527223.1:p.Ala909=
XM_011528922.2:c.2727C>T	XP_011527224.1:p.Ala909=
NM_020436.5:c.3033C>T MANE Select	NP_065169.1:p.Ala1011=
NM_001318031.2:c.1722C>T	NP_001304960.1:p.Ala574=