Canonical Allele Identifier: CA1207653965
Gene: TNFSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173206703C= , CM000663.2:g.173206703C= GRCh38
NC_000001.10:g.173175842C= , CM000663.1:g.173175842C= GRCh37
NC_000001.9:g.171442465C= NCBI36
NG_011477.1:g.5630G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.153+321G= MANE Select ENSP00000281834.3:n.153+321G=
ENST00000281834.3:c.153+321G= ENSP00000281834.3:n.153+321G=
NM_003326.4:c.153+321G= NP_003317.1:n.153+321G=
XM_011509964.1:c.225+321G= XP_011508266.1:n.225+321G=
XM_011509964.2:c.441+321G= XP_011508266.2:n.441+321G=
XM_017002228.1:c.-968G= XP_016857717.1:n.-968G=
XM_017002229.1:c.186+321G= XP_016857718.1:n.186+321G=
XM_017002230.1:c.180+321G= XP_016857719.1:n.180+321G=
NM_003326.5:c.153+321G= MANE Select NP_003317.1:n.153+321G=