Canonical Allele Identifier: CA590281549
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1329186361

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785425_114785427del , CM000671.2:g.114785425_114785427del GRCh38
NC_000009.11:g.117547705_117547707del , CM000671.1:g.117547705_117547707del GRCh37
NC_000009.10:g.116587526_116587528del NCBI36
NG_011488.2:g.25704_25706del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5027_*5029del MANE Select ENSP00000363157.3:n.*5027_*5029del
ENST00000374045.4:c.*5027_*5029del ENSP00000363157.3:n.*5027_*5029del
NM_001204344.1:c.5606_5608del NP_001191273.1:n.5606_5608del
NM_005118.3:c.*5027_*5029del NP_005109.2:n.*5027_*5029del
NM_005118.4:c.*5027_*5029del MANE Select NP_005109.2:n.*5027_*5029del