Canonical Allele Identifier: CA1874003185
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785459A= , CM000671.2:g.114785459A= GRCh38
NC_000009.11:g.117547739A= , CM000671.1:g.117547739A= GRCh37
NC_000009.10:g.116587560A= NCBI36
NG_011488.2:g.25670T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4993T= MANE Select ENSP00000363157.3:n.*4993T=
ENST00000374045.4:c.*4993T= ENSP00000363157.3:n.*4993T=
NM_001204344.1:c.5572T= NP_001191273.1:n.5572T=
NM_005118.3:c.*4993T= NP_005109.2:n.*4993T=
NM_005118.4:c.*4993T= MANE Select NP_005109.2:n.*4993T=