Canonical Allele Identifier: CA891270256
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1439725632

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173187054_173187059dup , CM000663.2:g.173187054_173187059dup GRCh38
NC_000001.10:g.173156193_173156198dup , CM000663.1:g.173156193_173156198dup GRCh37
NC_000001.9:g.171422816_171422821dup NCBI36
NG_011477.1:g.25277_25282dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.203-191_203-186dup MANE Select ENSP00000281834.3:n.203-191_203-186dup
ENST00000281834.3:c.203-191_203-186dup ENSP00000281834.3:n.203-191_203-186dup
ENST00000367718.5:c.53-191_53-186dup ENSP00000356691.1:n.53-191_53-186dup
NM_001297562.1:c.53-191_53-186dup NP_001284491.1:n.53-191_53-186dup
NM_003326.4:c.203-191_203-186dup NP_003317.1:n.203-191_203-186dup
XM_011509964.1:c.275-191_275-186dup XP_011508266.1:n.275-191_275-186dup
XM_011509964.2:c.491-191_491-186dup XP_011508266.2:n.491-191_491-186dup
XM_017002228.1:c.299-191_299-186dup XP_016857717.1:n.299-191_299-186dup
XM_017002229.1:c.236-191_236-186dup XP_016857718.1:n.236-191_236-186dup
XM_017002230.1:c.230-191_230-186dup XP_016857719.1:n.230-191_230-186dup
NM_003326.5:c.203-191_203-186dup MANE Select NP_003317.1:n.203-191_203-186dup
NM_001297562.2:c.53-191_53-186dup NP_001284491.1:n.53-191_53-186dup