Canonical Allele Identifier: CA1207645185

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187085_173187086delinsAG , CM000663.2:g.173187085_173187086delinsAG	GRCh38
NC_000001.10:g.173156224_173156225delinsAG , CM000663.1:g.173156224_173156225delinsAG	GRCh37
NC_000001.9:g.171422847_171422848delinsAG	NCBI36
NG_011477.1:g.25247_25248delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-221_203-220delinsCT MANE Select	ENSP00000281834.3:n.203-221_203-220delinsCT
ENST00000281834.3:c.203-221_203-220delinsCT	ENSP00000281834.3:n.203-221_203-220delinsCT
ENST00000367718.5:c.53-221_53-220delinsCT	ENSP00000356691.1:n.53-221_53-220delinsCT
NM_001297562.1:c.53-221_53-220delinsCT	NP_001284491.1:n.53-221_53-220delinsCT
NM_003326.4:c.203-221_203-220delinsCT	NP_003317.1:n.203-221_203-220delinsCT
XM_011509964.1:c.275-221_275-220delinsCT	XP_011508266.1:n.275-221_275-220delinsCT
XM_011509964.2:c.491-221_491-220delinsCT	XP_011508266.2:n.491-221_491-220delinsCT
XM_017002228.1:c.299-221_299-220delinsCT	XP_016857717.1:n.299-221_299-220delinsCT
XM_017002229.1:c.236-221_236-220delinsCT	XP_016857718.1:n.236-221_236-220delinsCT
XM_017002230.1:c.230-221_230-220delinsCT	XP_016857719.1:n.230-221_230-220delinsCT
NM_003326.5:c.203-221_203-220delinsCT MANE Select	NP_003317.1:n.203-221_203-220delinsCT
NM_001297562.2:c.53-221_53-220delinsCT	NP_001284491.1:n.53-221_53-220delinsCT