Canonical Allele Identifier: CA2369155235
Gene: SALL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.51784358G= , CM000682.2:g.51784358G= GRCh38
NC_000020.10:g.50400897G= , CM000682.1:g.50400897G= GRCh37
NC_000020.9:g.49834304G= NCBI36
NG_008000.1:g.23152C= , LRG_675:g.23152C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217086.9:c.3069C= MANE Select ENSP00000217086.4:p.Ile1023=
ENST00000217086.8:c.3069C= ENSP00000217086.4:p.Ile1023=
ENST00000371539.7:c.738C= ENSP00000360594.3:p.Ile246=
ENST00000395997.3:c.1758C= ENSP00000379319.3:p.Ile586=
NM_020436.3:c.3069C= , LRG_675t1:c.3069C= NP_065169.1:p.Ile1023=
XM_005260467.2:c.2763C= XP_005260524.1:p.Ile921=
XM_006723834.2:c.2763C= XP_006723897.1:p.Ile921=
XM_011528919.1:c.2943C= XP_011527221.1:p.Ile981=
XM_011528920.1:c.2763C= XP_011527222.1:p.Ile921=
XM_011528921.1:c.2763C= XP_011527223.1:p.Ile921=
XM_011528922.1:c.2763C= XP_011527224.1:p.Ile921=
XM_011528923.1:c.1758C= XP_011527225.1:p.Ile586=
NM_001318031.1:c.1758C= NP_001304960.1:p.Ile586=
NM_020436.4:c.3069C= NP_065169.1:p.Ile1023=
XM_005260467.4:c.2763C= XP_005260524.1:p.Ile921=
XM_011528921.2:c.2763C= XP_011527223.1:p.Ile921=
XM_011528922.2:c.2763C= XP_011527224.1:p.Ile921=
NM_020436.5:c.3069C= MANE Select NP_065169.1:p.Ile1023=
NM_001318031.2:c.1758C= NP_001304960.1:p.Ile586=