Canonical Allele Identifier: CA2542737865

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784177A>T , CM000682.2:g.51784177A>T	GRCh38
NC_000020.10:g.50400716A>T , CM000682.1:g.50400716A>T	GRCh37
NC_000020.9:g.49834123A>T	NCBI36
NG_008000.1:g.23333T>A , LRG_675:g.23333T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.*88T>A MANE Select	ENSP00000217086.4:n.*88T>A
ENST00000217086.8:c.*88T>A	ENSP00000217086.4:n.*88T>A
ENST00000371539.7:c.*88T>A	ENSP00000360594.3:n.*88T>A
NM_020436.3:c.*88T>A , LRG_675t1:c.*88T>A	NP_065169.1:n.*88T>A
XM_005260467.2:c.*88T>A	XP_005260524.1:n.*88T>A
XM_006723834.2:c.*88T>A	XP_006723897.1:n.*88T>A
XM_011528919.1:c.*88T>A	XP_011527221.1:n.*88T>A
XM_011528920.1:c.*88T>A	XP_011527222.1:n.*88T>A
XM_011528921.1:c.*88T>A	XP_011527223.1:n.*88T>A
XM_011528922.1:c.*88T>A	XP_011527224.1:n.*88T>A
XM_011528923.1:c.*88T>A	XP_011527225.1:n.*88T>A
NM_001318031.1:c.*88T>A	NP_001304960.1:n.*88T>A
NM_020436.4:c.*88T>A	NP_065169.1:n.*88T>A
XM_005260467.4:c.*88T>A	XP_005260524.1:n.*88T>A
XM_011528921.2:c.*88T>A	XP_011527223.1:n.*88T>A
XM_011528922.2:c.*88T>A	XP_011527224.1:n.*88T>A
NM_020436.5:c.*88T>A MANE Select	NP_065169.1:n.*88T>A
NM_001318031.2:c.*88T>A	NP_001304960.1:n.*88T>A