Canonical Allele Identifier: CA1207645137

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187054_173187062delinsCAAAAAAAA , CM000663.2:g.173187054_173187062delinsCAAAAAAAA	GRCh38
NC_000001.10:g.173156193_173156201delinsCAAAAAAAA , CM000663.1:g.173156193_173156201delinsCAAAAAAAA	GRCh37
NC_000001.9:g.171422816_171422824delinsCAAAAAAAA	NCBI36
NG_011477.1:g.25271_25279delinsTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-197_203-189delinsTTTTTTTTG MANE Select	ENSP00000281834.3:n.203-197_203-189delinsTTTTTTTTG
ENST00000281834.3:c.203-197_203-189delinsTTTTTTTTG	ENSP00000281834.3:n.203-197_203-189delinsTTTTTTTTG
ENST00000367718.5:c.53-197_53-189delinsTTTTTTTTG	ENSP00000356691.1:n.53-197_53-189delinsTTTTTTTTG
NM_001297562.1:c.53-197_53-189delinsTTTTTTTTG	NP_001284491.1:n.53-197_53-189delinsTTTTTTTTG
NM_003326.4:c.203-197_203-189delinsTTTTTTTTG	NP_003317.1:n.203-197_203-189delinsTTTTTTTTG
XM_011509964.1:c.275-197_275-189delinsTTTTTTTTG	XP_011508266.1:n.275-197_275-189delinsTTTTTTTTG
XM_011509964.2:c.491-197_491-189delinsTTTTTTTTG	XP_011508266.2:n.491-197_491-189delinsTTTTTTTTG
XM_017002228.1:c.299-197_299-189delinsTTTTTTTTG	XP_016857717.1:n.299-197_299-189delinsTTTTTTTTG
XM_017002229.1:c.236-197_236-189delinsTTTTTTTTG	XP_016857718.1:n.236-197_236-189delinsTTTTTTTTG
XM_017002230.1:c.230-197_230-189delinsTTTTTTTTG	XP_016857719.1:n.230-197_230-189delinsTTTTTTTTG
NM_003326.5:c.203-197_203-189delinsTTTTTTTTG MANE Select	NP_003317.1:n.203-197_203-189delinsTTTTTTTTG
NM_001297562.2:c.53-197_53-189delinsTTTTTTTTG	NP_001284491.1:n.53-197_53-189delinsTTTTTTTTG