Canonical Allele Identifier: CA1207653980
Gene: TNFSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173206743T= , CM000663.2:g.173206743T= GRCh38
NC_000001.10:g.173175882T= , CM000663.1:g.173175882T= GRCh37
NC_000001.9:g.171442505T= NCBI36
NG_011477.1:g.5590A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.153+281A= MANE Select ENSP00000281834.3:n.153+281A=
ENST00000281834.3:c.153+281A= ENSP00000281834.3:n.153+281A=
NM_003326.4:c.153+281A= NP_003317.1:n.153+281A=
XM_011509964.1:c.225+281A= XP_011508266.1:n.225+281A=
XM_011509964.2:c.441+281A= XP_011508266.2:n.441+281A=
XM_017002228.1:c.-1008A= XP_016857717.1:n.-1008A=
XM_017002229.1:c.186+281A= XP_016857718.1:n.186+281A=
XM_017002230.1:c.180+281A= XP_016857719.1:n.180+281A=
NM_003326.5:c.153+281A= MANE Select NP_003317.1:n.153+281A=