Canonical Allele Identifier: CA1207653974
Gene: TNFSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173206735A= , CM000663.2:g.173206735A= GRCh38
NC_000001.10:g.173175874A= , CM000663.1:g.173175874A= GRCh37
NC_000001.9:g.171442497A= NCBI36
NG_011477.1:g.5598T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.153+289T= MANE Select ENSP00000281834.3:n.153+289T=
ENST00000281834.3:c.153+289T= ENSP00000281834.3:n.153+289T=
NM_003326.4:c.153+289T= NP_003317.1:n.153+289T=
XM_011509964.1:c.225+289T= XP_011508266.1:n.225+289T=
XM_011509964.2:c.441+289T= XP_011508266.2:n.441+289T=
XM_017002228.1:c.-1000T= XP_016857717.1:n.-1000T=
XM_017002229.1:c.186+289T= XP_016857718.1:n.186+289T=
XM_017002230.1:c.180+289T= XP_016857719.1:n.180+289T=
NM_003326.5:c.153+289T= MANE Select NP_003317.1:n.153+289T=