Canonical Allele Identifier: CA1207653964

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1650207885

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173206699del , CM000663.2:g.173206699del	GRCh38
NC_000001.10:g.173175838del , CM000663.1:g.173175838del	GRCh37
NC_000001.9:g.171442461del	NCBI36
NG_011477.1:g.5634del

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+325del MANE Select	ENSP00000281834.3:n.153+325del
ENST00000281834.3:c.153+325del	ENSP00000281834.3:n.153+325del
NM_003326.4:c.153+325del	NP_003317.1:n.153+325del
XM_011509964.1:c.225+325del	XP_011508266.1:n.225+325del
XM_011509964.2:c.441+325del	XP_011508266.2:n.441+325del
XM_017002228.1:c.-964del	XP_016857717.1:n.-964del
XM_017002229.1:c.186+325del	XP_016857718.1:n.186+325del
XM_017002230.1:c.180+325del	XP_016857719.1:n.180+325del
NM_003326.5:c.153+325del MANE Select	NP_003317.1:n.153+325del