Canonical Allele Identifier: CA527602198

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1175157623
• gnomAD v2: 1-173156193-CAA-C
• gnomAD v3: 1-173187054-CAA-C
• gnomAD v4: 1-173187054-CAA-C
• MyVariant Identifiers: chr1:g.173156199_173156200del (hg19) ; chr1:g.173187060_173187061del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187065_173187066del , CM000663.2:g.173187065_173187066del	GRCh38
NC_000001.10:g.173156204_173156205del , CM000663.1:g.173156204_173156205del	GRCh37
NC_000001.9:g.171422827_171422828del	NCBI36
NG_011477.1:g.25277_25278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-191_203-190del MANE Select	ENSP00000281834.3:n.203-191_203-190del
ENST00000281834.3:c.203-191_203-190del	ENSP00000281834.3:n.203-191_203-190del
ENST00000367718.5:c.53-191_53-190del	ENSP00000356691.1:n.53-191_53-190del
NM_001297562.1:c.53-191_53-190del	NP_001284491.1:n.53-191_53-190del
NM_003326.4:c.203-191_203-190del	NP_003317.1:n.203-191_203-190del
XM_011509964.1:c.275-191_275-190del	XP_011508266.1:n.275-191_275-190del
XM_011509964.2:c.491-191_491-190del	XP_011508266.2:n.491-191_491-190del
XM_017002228.1:c.299-191_299-190del	XP_016857717.1:n.299-191_299-190del
XM_017002229.1:c.236-191_236-190del	XP_016857718.1:n.236-191_236-190del
XM_017002230.1:c.230-191_230-190del	XP_016857719.1:n.230-191_230-190del
NM_003326.5:c.203-191_203-190del MANE Select	NP_003317.1:n.203-191_203-190del
NM_001297562.2:c.53-191_53-190del	NP_001284491.1:n.53-191_53-190del