Canonical Allele Identifier: CA2746672834

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173201401_173201409del , CM000663.2:g.173201401_173201409del	GRCh38
NC_000001.10:g.173170540_173170548del , CM000663.1:g.173170540_173170548del	GRCh37
NC_000001.9:g.171437163_171437171del	NCBI36
NG_011477.1:g.10927_10935del

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+5618_153+5626del MANE Select	ENSP00000281834.3:n.153+5618_153+5626del
ENST00000281834.3:c.153+5618_153+5626del	ENSP00000281834.3:n.153+5618_153+5626del
ENST00000367718.5:c.3+3905_3+3913del	ENSP00000356691.1:n.3+3905_3+3913del
ENST00000488053.1:n.414+3905_414+3913del
NM_001297562.1:c.3+3905_3+3913del	NP_001284491.1:n.3+3905_3+3913del
NM_003326.4:c.153+5618_153+5626del	NP_003317.1:n.153+5618_153+5626del
XM_011509964.1:c.225+5618_225+5626del	XP_011508266.1:n.225+5618_225+5626del
XM_011509964.2:c.441+5618_441+5626del	XP_011508266.2:n.441+5618_441+5626del
XM_017002228.1:c.249+4081_249+4089del	XP_016857717.1:n.249+4081_249+4089del
XM_017002229.1:c.186+5618_186+5626del	XP_016857718.1:n.186+5618_186+5626del
XM_017002230.1:c.180+5618_180+5626del	XP_016857719.1:n.180+5618_180+5626del
NM_003326.5:c.153+5618_153+5626del MANE Select	NP_003317.1:n.153+5618_153+5626del
NM_001297562.2:c.3+3905_3+3913del	NP_001284491.1:n.3+3905_3+3913del