Canonical Allele Identifier: CA2816661613

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784823_51784824insAGA , CM000682.2:g.51784823_51784824insAGA	GRCh38
NC_000020.10:g.50401362_50401363insAGA , CM000682.1:g.50401362_50401363insAGA	GRCh37
NC_000020.9:g.49834769_49834770insAGA	NCBI36
NG_008000.1:g.22686_22687insTCT , LRG_675:g.22686_22687insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2743-140_2743-139insTCT MANE Select	ENSP00000217086.4:n.2743-140_2743-139insTCT
ENST00000217086.8:c.2743-140_2743-139insTCT	ENSP00000217086.4:n.2743-140_2743-139insTCT
ENST00000371539.7:c.412-140_412-139insTCT	ENSP00000360594.3:n.412-140_412-139insTCT
ENST00000395997.3:c.1432-140_1432-139insTCT	ENSP00000379319.3:n.1432-140_1432-139insTCT
NM_020436.3:c.2743-140_2743-139insTCT , LRG_675t1:c.2743-140_2743-139insTCT	NP_065169.1:n.2743-140_2743-139insTCT
XM_005260467.2:c.2437-140_2437-139insTCT	XP_005260524.1:n.2437-140_2437-139insTCT
XM_006723834.2:c.2437-140_2437-139insTCT	XP_006723897.1:n.2437-140_2437-139insTCT
XM_011528919.1:c.2617-140_2617-139insTCT	XP_011527221.1:n.2617-140_2617-139insTCT
XM_011528920.1:c.2437-140_2437-139insTCT	XP_011527222.1:n.2437-140_2437-139insTCT
XM_011528921.1:c.2437-140_2437-139insTCT	XP_011527223.1:n.2437-140_2437-139insTCT
XM_011528922.1:c.2437-140_2437-139insTCT	XP_011527224.1:n.2437-140_2437-139insTCT
XM_011528923.1:c.1432-140_1432-139insTCT	XP_011527225.1:n.1432-140_1432-139insTCT
NM_001318031.1:c.1432-140_1432-139insTCT	NP_001304960.1:n.1432-140_1432-139insTCT
NM_020436.4:c.2743-140_2743-139insTCT	NP_065169.1:n.2743-140_2743-139insTCT
XM_005260467.4:c.2437-140_2437-139insTCT	XP_005260524.1:n.2437-140_2437-139insTCT
XM_011528921.2:c.2437-140_2437-139insTCT	XP_011527223.1:n.2437-140_2437-139insTCT
XM_011528922.2:c.2437-140_2437-139insTCT	XP_011527224.1:n.2437-140_2437-139insTCT
NM_020436.5:c.2743-140_2743-139insTCT MANE Select	NP_065169.1:n.2743-140_2743-139insTCT
NM_001318031.2:c.1432-140_1432-139insTCT	NP_001304960.1:n.1432-140_1432-139insTCT