Canonical Allele Identifier: CA1874003256
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785502A= , CM000671.2:g.114785502A= GRCh38
NC_000009.11:g.117547782A= , CM000671.1:g.117547782A= GRCh37
NC_000009.10:g.116587603A= NCBI36
NG_011488.2:g.25627T=

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.*4950T= MANE Select ENSP00000363157.3:n.*4950T=
ENST00000374045.4:c.*4950T= ENSP00000363157.3:n.*4950T=
NM_001204344.1:c.5529T= NP_001191273.1:n.5529T=
NM_005118.3:c.*4950T= NP_005109.2:n.*4950T=
NM_005118.4:c.*4950T= MANE Select NP_005109.2:n.*4950T=