Canonical Allele Identifier: CA15133070
Gene: TNFSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173197108A>G , CM000663.2:g.173197108A>G GRCh38
NC_000001.10:g.173166247A>G , CM000663.1:g.173166247A>G GRCh37
NC_000001.9:g.171432870A>G NCBI36
NG_011477.1:g.15225T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.154-8539T>C MANE Select ENSP00000281834.3:n.154-8539T>C
ENST00000281834.3:c.154-8539T>C ENSP00000281834.3:n.154-8539T>C
ENST00000367718.5:c.3+8203T>C ENSP00000356691.1:n.3+8203T>C
ENST00000488053.1:n.414+8203T>C
NM_001297562.1:c.3+8203T>C NP_001284491.1:n.3+8203T>C
NM_003326.4:c.154-8539T>C NP_003317.1:n.154-8539T>C
XM_011509964.1:c.226-8539T>C XP_011508266.1:n.226-8539T>C
XM_011509964.2:c.442-8539T>C XP_011508266.2:n.442-8539T>C
XM_017002228.1:c.249+8379T>C XP_016857717.1:n.249+8379T>C
XM_017002229.1:c.187-8539T>C XP_016857718.1:n.187-8539T>C
XM_017002230.1:c.181-8539T>C XP_016857719.1:n.181-8539T>C
NM_003326.5:c.154-8539T>C MANE Select NP_003317.1:n.154-8539T>C
NM_001297562.2:c.3+8203T>C NP_001284491.1:n.3+8203T>C