Canonical Allele Identifier: CA1009207533

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1650208341
• gnomAD v3: 1-173206720-CA-C
• gnomAD v4: 1-173206720-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173206723del , CM000663.2:g.173206723del	GRCh38
NC_000001.10:g.173175862del , CM000663.1:g.173175862del	GRCh37
NC_000001.9:g.171442485del	NCBI36
NG_011477.1:g.5612del

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+303del MANE Select	ENSP00000281834.3:n.153+303del
ENST00000281834.3:c.153+303del	ENSP00000281834.3:n.153+303del
NM_003326.4:c.153+303del	NP_003317.1:n.153+303del
XM_011509964.1:c.225+303del	XP_011508266.1:n.225+303del
XM_011509964.2:c.441+303del	XP_011508266.2:n.441+303del
XM_017002228.1:c.-986del	XP_016857717.1:n.-986del
XM_017002229.1:c.186+303del	XP_016857718.1:n.186+303del
XM_017002230.1:c.180+303del	XP_016857719.1:n.180+303del
NM_003326.5:c.153+303del MANE Select	NP_003317.1:n.153+303del