Canonical Allele Identifier: CA1207645492

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187537_173187538delinsTG , CM000663.2:g.173187537_173187538delinsTG	GRCh38
NC_000001.10:g.173156676_173156677delinsTG , CM000663.1:g.173156676_173156677delinsTG	GRCh37
NC_000001.9:g.171423299_171423300delinsTG	NCBI36
NG_011477.1:g.24795_24796delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-673_203-672delinsCA MANE Select	ENSP00000281834.3:n.203-673_203-672delinsCA
ENST00000281834.3:c.203-673_203-672delinsCA	ENSP00000281834.3:n.203-673_203-672delinsCA
ENST00000367718.5:c.53-673_53-672delinsCA	ENSP00000356691.1:n.53-673_53-672delinsCA
NM_001297562.1:c.53-673_53-672delinsCA	NP_001284491.1:n.53-673_53-672delinsCA
NM_003326.4:c.203-673_203-672delinsCA	NP_003317.1:n.203-673_203-672delinsCA
XM_011509964.1:c.275-673_275-672delinsCA	XP_011508266.1:n.275-673_275-672delinsCA
XM_011509964.2:c.491-673_491-672delinsCA	XP_011508266.2:n.491-673_491-672delinsCA
XM_017002228.1:c.299-673_299-672delinsCA	XP_016857717.1:n.299-673_299-672delinsCA
XM_017002229.1:c.236-673_236-672delinsCA	XP_016857718.1:n.236-673_236-672delinsCA
XM_017002230.1:c.230-673_230-672delinsCA	XP_016857719.1:n.230-673_230-672delinsCA
NM_003326.5:c.203-673_203-672delinsCA MANE Select	NP_003317.1:n.203-673_203-672delinsCA
NM_001297562.2:c.53-673_53-672delinsCA	NP_001284491.1:n.53-673_53-672delinsCA