Canonical Allele Identifier: CA1207653971
Gene: TNFSF4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173206732G= , CM000663.2:g.173206732G= GRCh38
NC_000001.10:g.173175871G= , CM000663.1:g.173175871G= GRCh37
NC_000001.9:g.171442494G= NCBI36
NG_011477.1:g.5601C=

Transcript Alleles

HGVS Amino-acid change
ENST00000281834.4:c.153+292C= MANE Select ENSP00000281834.3:n.153+292C=
ENST00000281834.3:c.153+292C= ENSP00000281834.3:n.153+292C=
NM_003326.4:c.153+292C= NP_003317.1:n.153+292C=
XM_011509964.1:c.225+292C= XP_011508266.1:n.225+292C=
XM_011509964.2:c.441+292C= XP_011508266.2:n.441+292C=
XM_017002228.1:c.-997C= XP_016857717.1:n.-997C=
XM_017002229.1:c.186+292C= XP_016857718.1:n.186+292C=
XM_017002230.1:c.180+292C= XP_016857719.1:n.180+292C=
NM_003326.5:c.153+292C= MANE Select NP_003317.1:n.153+292C=
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