Canonical Allele Identifier: CA1009221443

Gene: TNFSF4

Linked Data

• gnomAD v3: 1-173187050-C-CA
• gnomAD v4: 1-173187050-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187053dup , CM000663.2:g.173187053dup	GRCh38
NC_000001.10:g.173156192dup , CM000663.1:g.173156192dup	GRCh37
NC_000001.9:g.171422815dup	NCBI36
NG_011477.1:g.25282dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-186dup MANE Select	ENSP00000281834.3:n.203-186dup
ENST00000281834.3:c.203-186dup	ENSP00000281834.3:n.203-186dup
ENST00000367718.5:c.53-186dup	ENSP00000356691.1:n.53-186dup
NM_001297562.1:c.53-186dup	NP_001284491.1:n.53-186dup
NM_003326.4:c.203-186dup	NP_003317.1:n.203-186dup
XM_011509964.1:c.275-186dup	XP_011508266.1:n.275-186dup
XM_011509964.2:c.491-186dup	XP_011508266.2:n.491-186dup
XM_017002228.1:c.299-186dup	XP_016857717.1:n.299-186dup
XM_017002229.1:c.236-186dup	XP_016857718.1:n.236-186dup
XM_017002230.1:c.230-186dup	XP_016857719.1:n.230-186dup
NM_003326.5:c.203-186dup MANE Select	NP_003317.1:n.203-186dup
NM_001297562.2:c.53-186dup	NP_001284491.1:n.53-186dup