Canonical Allele Identifier: CA2816661632

Gene: SALL4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.51784846_51784853del , CM000682.2:g.51784846_51784853del	GRCh38
NC_000020.10:g.50401385_50401392del , CM000682.1:g.50401385_50401392del	GRCh37
NC_000020.9:g.49834792_49834799del	NCBI36
NG_008000.1:g.22657_22664del , LRG_675:g.22657_22664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217086.9:c.2743-169_2743-162del MANE Select	ENSP00000217086.4:n.2743-169_2743-162del
ENST00000217086.8:c.2743-169_2743-162del	ENSP00000217086.4:n.2743-169_2743-162del
ENST00000371539.7:c.412-169_412-162del	ENSP00000360594.3:n.412-169_412-162del
ENST00000395997.3:c.1432-169_1432-162del	ENSP00000379319.3:n.1432-169_1432-162del
NM_020436.3:c.2743-169_2743-162del , LRG_675t1:c.2743-169_2743-162del	NP_065169.1:n.2743-169_2743-162del
XM_005260467.2:c.2437-169_2437-162del	XP_005260524.1:n.2437-169_2437-162del
XM_006723834.2:c.2437-169_2437-162del	XP_006723897.1:n.2437-169_2437-162del
XM_011528919.1:c.2617-169_2617-162del	XP_011527221.1:n.2617-169_2617-162del
XM_011528920.1:c.2437-169_2437-162del	XP_011527222.1:n.2437-169_2437-162del
XM_011528921.1:c.2437-169_2437-162del	XP_011527223.1:n.2437-169_2437-162del
XM_011528922.1:c.2437-169_2437-162del	XP_011527224.1:n.2437-169_2437-162del
XM_011528923.1:c.1432-169_1432-162del	XP_011527225.1:n.1432-169_1432-162del
NM_001318031.1:c.1432-169_1432-162del	NP_001304960.1:n.1432-169_1432-162del
NM_020436.4:c.2743-169_2743-162del	NP_065169.1:n.2743-169_2743-162del
XM_005260467.4:c.2437-169_2437-162del	XP_005260524.1:n.2437-169_2437-162del
XM_011528921.2:c.2437-169_2437-162del	XP_011527223.1:n.2437-169_2437-162del
XM_011528922.2:c.2437-169_2437-162del	XP_011527224.1:n.2437-169_2437-162del
NM_020436.5:c.2743-169_2743-162del MANE Select	NP_065169.1:n.2743-169_2743-162del
NM_001318031.2:c.1432-169_1432-162del	NP_001304960.1:n.1432-169_1432-162del