Canonical Allele Identifier: CA1207645127

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187048_173187065delinsCTCAAACAAAAAAAAAAA , CM000663.2:g.173187048_173187065delinsCTCAAACAAAAAAAAAAA	GRCh38
NC_000001.10:g.173156187_173156204delinsCTCAAACAAAAAAAAAAA , CM000663.1:g.173156187_173156204delinsCTCAAACAAAAAAAAAAA	GRCh37
NC_000001.9:g.171422810_171422827delinsCTCAAACAAAAAAAAAAA	NCBI36
NG_011477.1:g.25268_25285delinsTTTTTTTTTTTGTTTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-200_203-183delinsTTTTTTTTTTTGTTTGAG MANE Select	ENSP00000281834.3:n.203-200_203-183delinsTTTTTTTTTTTGTTTGAG
ENST00000281834.3:c.203-200_203-183delinsTTTTTTTTTTTGTTTGAG	ENSP00000281834.3:n.203-200_203-183delinsTTTTTTTTTTTGTTTGAG
ENST00000367718.5:c.53-200_53-183delinsTTTTTTTTTTTGTTTGAG	ENSP00000356691.1:n.53-200_53-183delinsTTTTTTTTTTTGTTTGAG
NM_001297562.1:c.53-200_53-183delinsTTTTTTTTTTTGTTTGAG	NP_001284491.1:n.53-200_53-183delinsTTTTTTTTTTTGTTTGAG
NM_003326.4:c.203-200_203-183delinsTTTTTTTTTTTGTTTGAG	NP_003317.1:n.203-200_203-183delinsTTTTTTTTTTTGTTTGAG
XM_011509964.1:c.275-200_275-183delinsTTTTTTTTTTTGTTTGAG	XP_011508266.1:n.275-200_275-183delinsTTTTTTTTTTTGTTTGAG
XM_011509964.2:c.491-200_491-183delinsTTTTTTTTTTTGTTTGAG	XP_011508266.2:n.491-200_491-183delinsTTTTTTTTTTTGTTTGAG
XM_017002228.1:c.299-200_299-183delinsTTTTTTTTTTTGTTTGAG	XP_016857717.1:n.299-200_299-183delinsTTTTTTTTTTTGTTTGAG
XM_017002229.1:c.236-200_236-183delinsTTTTTTTTTTTGTTTGAG	XP_016857718.1:n.236-200_236-183delinsTTTTTTTTTTTGTTTGAG
XM_017002230.1:c.230-200_230-183delinsTTTTTTTTTTTGTTTGAG	XP_016857719.1:n.230-200_230-183delinsTTTTTTTTTTTGTTTGAG
NM_003326.5:c.203-200_203-183delinsTTTTTTTTTTTGTTTGAG MANE Select	NP_003317.1:n.203-200_203-183delinsTTTTTTTTTTTGTTTGAG
NM_001297562.2:c.53-200_53-183delinsTTTTTTTTTTTGTTTGAG	NP_001284491.1:n.53-200_53-183delinsTTTTTTTTTTTGTTTGAG