Canonical Allele Identifier: CA1009221447

Gene: TNFSF4

Linked Data

• gnomAD v3: 1-173187054-CAAA-C
• gnomAD v4: 1-173187054-CAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187064_173187066del , CM000663.2:g.173187064_173187066del	GRCh38
NC_000001.10:g.173156203_173156205del , CM000663.1:g.173156203_173156205del	GRCh37
NC_000001.9:g.171422826_171422828del	NCBI36
NG_011477.1:g.25276_25278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-192_203-190del MANE Select	ENSP00000281834.3:n.203-192_203-190del
ENST00000281834.3:c.203-192_203-190del	ENSP00000281834.3:n.203-192_203-190del
ENST00000367718.5:c.53-192_53-190del	ENSP00000356691.1:n.53-192_53-190del
NM_001297562.1:c.53-192_53-190del	NP_001284491.1:n.53-192_53-190del
NM_003326.4:c.203-192_203-190del	NP_003317.1:n.203-192_203-190del
XM_011509964.1:c.275-192_275-190del	XP_011508266.1:n.275-192_275-190del
XM_011509964.2:c.491-192_491-190del	XP_011508266.2:n.491-192_491-190del
XM_017002228.1:c.299-192_299-190del	XP_016857717.1:n.299-192_299-190del
XM_017002229.1:c.236-192_236-190del	XP_016857718.1:n.236-192_236-190del
XM_017002230.1:c.230-192_230-190del	XP_016857719.1:n.230-192_230-190del
NM_003326.5:c.203-192_203-190del MANE Select	NP_003317.1:n.203-192_203-190del
NM_001297562.2:c.53-192_53-190del	NP_001284491.1:n.53-192_53-190del