Canonical Allele Identifier: CA891276773
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1272269701
gnomAD v3: 1-173206694-TG-T
gnomAD v4: 1-173206694-TG-T
MyVariant Identifiers: chr1:g.173175834del (hg19) chr1:g.173206695del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173206697del , CM000663.2:g.173206697del GRCh38
NC_000001.10:g.173175836del , CM000663.1:g.173175836del GRCh37
NC_000001.9:g.171442459del NCBI36
NG_011477.1:g.5638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.153+329del MANE Select ENSP00000281834.3:n.153+329del
ENST00000281834.3:c.153+329del ENSP00000281834.3:n.153+329del
NM_003326.4:c.153+329del NP_003317.1:n.153+329del
XM_011509964.1:c.225+329del XP_011508266.1:n.225+329del
XM_011509964.2:c.441+329del XP_011508266.2:n.441+329del
XM_017002228.1:c.-960del XP_016857717.1:n.-960del
XM_017002229.1:c.186+329del XP_016857718.1:n.186+329del
XM_017002230.1:c.180+329del XP_016857719.1:n.180+329del
NM_003326.5:c.153+329del MANE Select NP_003317.1:n.153+329del
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