Canonical Allele Identifier: CA2653358915

Gene: SALL4

Linked Data

• gnomAD v4: 20-51788806-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51788806T>G , CM000682.2:g.51788806T>G	GRCh38
NC_000020.10:g.50405345T>G , CM000682.1:g.50405345T>G	GRCh37
NC_000020.9:g.49838752T>G	NCBI36
NG_008000.1:g.18704A>C , LRG_675:g.18704A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000217086.9:c.2742+55A>C MANE Select	ENSP00000217086.4:n.2742+55A>C
ENST00000217086.8:c.2742+55A>C	ENSP00000217086.4:n.2742+55A>C
ENST00000371539.7:c.411+55A>C	ENSP00000360594.3:n.411+55A>C
ENST00000395997.3:c.1431+55A>C	ENSP00000379319.3:n.1431+55A>C
NM_020436.3:c.2742+55A>C , LRG_675t1:c.2742+55A>C	NP_065169.1:n.2742+55A>C
XM_005260467.2:c.2436+55A>C	XP_005260524.1:n.2436+55A>C
XM_006723834.2:c.2436+55A>C	XP_006723897.1:n.2436+55A>C
XM_011528919.1:c.2616+55A>C	XP_011527221.1:n.2616+55A>C
XM_011528920.1:c.2436+55A>C	XP_011527222.1:n.2436+55A>C
XM_011528921.1:c.2436+55A>C	XP_011527223.1:n.2436+55A>C
XM_011528922.1:c.2436+55A>C	XP_011527224.1:n.2436+55A>C
XM_011528923.1:c.1431+55A>C	XP_011527225.1:n.1431+55A>C
NM_001318031.1:c.1431+55A>C	NP_001304960.1:n.1431+55A>C
NM_020436.4:c.2742+55A>C	NP_065169.1:n.2742+55A>C
XM_005260467.4:c.2436+55A>C	XP_005260524.1:n.2436+55A>C
XM_011528921.2:c.2436+55A>C	XP_011527223.1:n.2436+55A>C
XM_011528922.2:c.2436+55A>C	XP_011527224.1:n.2436+55A>C
NM_020436.5:c.2742+55A>C MANE Select	NP_065169.1:n.2742+55A>C
NM_001318031.2:c.1431+55A>C	NP_001304960.1:n.1431+55A>C