Canonical Allele Identifier: CA858969422
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1293291722
MyVariant Identifiers: chr9:g.117547748_117547752del (hg19) chr9:g.114785468_114785472del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785468_114785472del , CM000671.2:g.114785468_114785472del GRCh38
NC_000009.11:g.117547748_117547752del , CM000671.1:g.117547748_117547752del GRCh37
NC_000009.10:g.116587569_116587573del NCBI36
NG_011488.2:g.25657_25661del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4980_*4984del MANE Select ENSP00000363157.3:n.*4980_*4984del
ENST00000374045.4:c.*4980_*4984del ENSP00000363157.3:n.*4980_*4984del
NM_001204344.1:c.5559_5563del NP_001191273.1:n.5559_5563del
NM_005118.3:c.*4980_*4984del NP_005109.2:n.*4980_*4984del
NM_005118.4:c.*4980_*4984del MANE Select NP_005109.2:n.*4980_*4984del
Search 100 bp 5'
Search 100 bp 3'