Canonical Allele Identifier: CA1140216776

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173201479C= , CM000663.2:g.173201479C=	GRCh38
NC_000001.10:g.173170618C= , CM000663.1:g.173170618C=	GRCh37
NC_000001.9:g.171437241C=	NCBI36
NG_011477.1:g.10854G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.153+5545G= MANE Select	ENSP00000281834.3:n.153+5545G=
ENST00000281834.3:c.153+5545G=	ENSP00000281834.3:n.153+5545G=
ENST00000367718.5:c.3+3832G=	ENSP00000356691.1:n.3+3832G=
ENST00000488053.1:n.414+3832G=
NM_001297562.1:c.3+3832G=	NP_001284491.1:n.3+3832G=
NM_003326.4:c.153+5545G=	NP_003317.1:n.153+5545G=
XM_011509964.1:c.225+5545G=	XP_011508266.1:n.225+5545G=
XM_011509964.2:c.441+5545G=	XP_011508266.2:n.441+5545G=
XM_017002228.1:c.249+4008G=	XP_016857717.1:n.249+4008G=
XM_017002229.1:c.186+5545G=	XP_016857718.1:n.186+5545G=
XM_017002230.1:c.180+5545G=	XP_016857719.1:n.180+5545G=
NM_003326.5:c.153+5545G= MANE Select	NP_003317.1:n.153+5545G=
NM_001297562.2:c.3+3832G=	NP_001284491.1:n.3+3832G=