Canonical Allele Identifier: CA1139859241

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173197108A= , CM000663.2:g.173197108A=	GRCh38
NC_000001.10:g.173166247A= , CM000663.1:g.173166247A=	GRCh37
NC_000001.9:g.171432870A=	NCBI36
NG_011477.1:g.15225T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.154-8539T= MANE Select	ENSP00000281834.3:n.154-8539T=
ENST00000281834.3:c.154-8539T=	ENSP00000281834.3:n.154-8539T=
ENST00000367718.5:c.3+8203T=	ENSP00000356691.1:n.3+8203T=
ENST00000488053.1:n.414+8203T=
NM_001297562.1:c.3+8203T=	NP_001284491.1:n.3+8203T=
NM_003326.4:c.154-8539T=	NP_003317.1:n.154-8539T=
XM_011509964.1:c.226-8539T=	XP_011508266.1:n.226-8539T=
XM_011509964.2:c.442-8539T=	XP_011508266.2:n.442-8539T=
XM_017002228.1:c.249+8379T=	XP_016857717.1:n.249+8379T=
XM_017002229.1:c.187-8539T=	XP_016857718.1:n.187-8539T=
XM_017002230.1:c.181-8539T=	XP_016857719.1:n.181-8539T=
NM_003326.5:c.154-8539T= MANE Select	NP_003317.1:n.154-8539T=
NM_001297562.2:c.3+8203T=	NP_001284491.1:n.3+8203T=