Canonical Allele Identifier: CA2519405304
Gene: TNFSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173187054del , CM000663.2:g.173187054del GRCh38
NC_000001.10:g.173156193del , CM000663.1:g.173156193del GRCh37
NC_000001.9:g.171422816del NCBI36
NG_011477.1:g.25279del

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.203-189del MANE Select ENSP00000281834.3:n.203-189del
ENST00000281834.3:c.203-189del ENSP00000281834.3:n.203-189del
ENST00000367718.5:c.53-189del ENSP00000356691.1:n.53-189del
NM_001297562.1:c.53-189del NP_001284491.1:n.53-189del
NM_003326.4:c.203-189del NP_003317.1:n.203-189del
XM_011509964.1:c.275-189del XP_011508266.1:n.275-189del
XM_011509964.2:c.491-189del XP_011508266.2:n.491-189del
XM_017002228.1:c.299-189del XP_016857717.1:n.299-189del
XM_017002229.1:c.236-189del XP_016857718.1:n.236-189del
XM_017002230.1:c.230-189del XP_016857719.1:n.230-189del
NM_003326.5:c.203-189del MANE Select NP_003317.1:n.203-189del
NM_001297562.2:c.53-189del NP_001284491.1:n.53-189del