Canonical Allele Identifier: CA1207653973
Gene: TNFSF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173206734G= , CM000663.2:g.173206734G= GRCh38
NC_000001.10:g.173175873G= , CM000663.1:g.173175873G= GRCh37
NC_000001.9:g.171442496G= NCBI36
NG_011477.1:g.5599C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.153+290C= MANE Select ENSP00000281834.3:n.153+290C=
ENST00000281834.3:c.153+290C= ENSP00000281834.3:n.153+290C=
NM_003326.4:c.153+290C= NP_003317.1:n.153+290C=
XM_011509964.1:c.225+290C= XP_011508266.1:n.225+290C=
XM_011509964.2:c.441+290C= XP_011508266.2:n.441+290C=
XM_017002228.1:c.-999C= XP_016857717.1:n.-999C=
XM_017002229.1:c.186+290C= XP_016857718.1:n.186+290C=
XM_017002230.1:c.180+290C= XP_016857719.1:n.180+290C=
NM_003326.5:c.153+290C= MANE Select NP_003317.1:n.153+290C=