Canonical Allele Identifier: CA2369157353
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51788975C= , CM000682.2:g.51788975C= GRCh38
NC_000020.10:g.50405514C= , CM000682.1:g.50405514C= GRCh37
NC_000020.9:g.49838921C= NCBI36
NG_008000.1:g.18535G= , LRG_675:g.18535G=

Transcript Alleles

HGVS Amino-acid change
ENST00000217086.9:c.2628G= MANE Select ENSP00000217086.4:p.Gly876=
ENST00000217086.8:c.2628G= ENSP00000217086.4:p.Gly876=
ENST00000371539.7:c.297G= ENSP00000360594.3:p.Gly99=
ENST00000395997.3:c.1317G= ENSP00000379319.3:p.Gly439=
NM_020436.3:c.2628G= , LRG_675t1:c.2628G= NP_065169.1:p.Gly876=
XM_005260467.2:c.2322G= XP_005260524.1:p.Gly774=
XM_006723834.2:c.2322G= XP_006723897.1:p.Gly774=
XM_011528919.1:c.2502G= XP_011527221.1:p.Gly834=
XM_011528920.1:c.2322G= XP_011527222.1:p.Gly774=
XM_011528921.1:c.2322G= XP_011527223.1:p.Gly774=
XM_011528922.1:c.2322G= XP_011527224.1:p.Gly774=
XM_011528923.1:c.1317G= XP_011527225.1:p.Gly439=
NM_001318031.1:c.1317G= NP_001304960.1:p.Gly439=
NM_020436.4:c.2628G= NP_065169.1:p.Gly876=
XM_005260467.4:c.2322G= XP_005260524.1:p.Gly774=
XM_011528921.2:c.2322G= XP_011527223.1:p.Gly774=
XM_011528922.2:c.2322G= XP_011527224.1:p.Gly774=
NM_020436.5:c.2628G= MANE Select NP_065169.1:p.Gly876=
NM_001318031.2:c.1317G= NP_001304960.1:p.Gly439=