Canonical Allele Identifier: CA2369155149

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784186G= , CM000682.2:g.51784186G=	GRCh38
NC_000020.10:g.50400725G= , CM000682.1:g.50400725G=	GRCh37
NC_000020.9:g.49834132G=	NCBI36
NG_008000.1:g.23324C= , LRG_675:g.23324C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.*79C= MANE Select	ENSP00000217086.4:n.*79C=
ENST00000217086.8:c.*79C=	ENSP00000217086.4:n.*79C=
ENST00000371539.7:c.*79C=	ENSP00000360594.3:n.*79C=
NM_020436.3:c.*79C= , LRG_675t1:c.*79C=	NP_065169.1:n.*79C=
XM_005260467.2:c.*79C=	XP_005260524.1:n.*79C=
XM_006723834.2:c.*79C=	XP_006723897.1:n.*79C=
XM_011528919.1:c.*79C=	XP_011527221.1:n.*79C=
XM_011528920.1:c.*79C=	XP_011527222.1:n.*79C=
XM_011528921.1:c.*79C=	XP_011527223.1:n.*79C=
XM_011528922.1:c.*79C=	XP_011527224.1:n.*79C=
XM_011528923.1:c.*79C=	XP_011527225.1:n.*79C=
NM_001318031.1:c.*79C=	NP_001304960.1:n.*79C=
NM_020436.4:c.*79C=	NP_065169.1:n.*79C=
XM_005260467.4:c.*79C=	XP_005260524.1:n.*79C=
XM_011528921.2:c.*79C=	XP_011527223.1:n.*79C=
XM_011528922.2:c.*79C=	XP_011527224.1:n.*79C=
NM_020436.5:c.*79C= MANE Select	NP_065169.1:n.*79C=
NM_001318031.2:c.*79C=	NP_001304960.1:n.*79C=