Canonical Allele Identifier: CA1207653977

Gene: TNFSF4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173206741T= , CM000663.2:g.173206741T=	GRCh38
NC_000001.10:g.173175880T= , CM000663.1:g.173175880T=	GRCh37
NC_000001.9:g.171442503T=	NCBI36
NG_011477.1:g.5592A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+283A= MANE Select	ENSP00000281834.3:n.153+283A=
ENST00000281834.3:c.153+283A=	ENSP00000281834.3:n.153+283A=
NM_003326.4:c.153+283A=	NP_003317.1:n.153+283A=
XM_011509964.1:c.225+283A=	XP_011508266.1:n.225+283A=
XM_011509964.2:c.441+283A=	XP_011508266.2:n.441+283A=
XM_017002228.1:c.-1006A=	XP_016857717.1:n.-1006A=
XM_017002229.1:c.186+283A=	XP_016857718.1:n.186+283A=
XM_017002230.1:c.180+283A=	XP_016857719.1:n.180+283A=
NM_003326.5:c.153+283A= MANE Select	NP_003317.1:n.153+283A=