Canonical Allele Identifier: CA15085808
Gene: TNFSF4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173185165G>T , CM000663.2:g.173185165G>T GRCh38
NC_000001.10:g.173154304G>T , CM000663.1:g.173154304G>T GRCh37
NC_000001.9:g.171420927G>T NCBI36
NG_011477.1:g.27168C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.*1351C>A MANE Select ENSP00000281834.3:n.*1351C>A
ENST00000281834.3:c.*1351C>A ENSP00000281834.3:n.*1351C>A
ENST00000367718.5:c.*1351C>A ENSP00000356691.1:n.*1351C>A
NM_001297562.1:c.*1351C>A NP_001284491.1:n.*1351C>A
NM_003326.4:c.*1351C>A NP_003317.1:n.*1351C>A
XM_011509964.1:c.*1351C>A XP_011508266.1:n.*1351C>A
XM_011509964.2:c.*1351C>A XP_011508266.2:n.*1351C>A
XM_017002228.1:c.*1351C>A XP_016857717.1:n.*1351C>A
XM_017002229.1:c.*1351C>A XP_016857718.1:n.*1351C>A
XM_017002230.1:c.*1351C>A XP_016857719.1:n.*1351C>A
NM_003326.5:c.*1351C>A MANE Select NP_003317.1:n.*1351C>A
NM_001297562.2:c.*1351C>A NP_001284491.1:n.*1351C>A
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