Canonical Allele Identifier: CA1874003056
Gene: TNFSF15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785351A= , CM000671.2:g.114785351A= GRCh38
NC_000009.11:g.117547631A= , CM000671.1:g.117547631A= GRCh37
NC_000009.10:g.116587452A= NCBI36
NG_011488.2:g.25778T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5101T= MANE Select ENSP00000363157.3:n.*5101T=
ENST00000374045.4:c.*5101T= ENSP00000363157.3:n.*5101T=
NM_001204344.1:c.5680T= NP_001191273.1:n.5680T=
NM_005118.3:c.*5101T= NP_005109.2:n.*5101T=
NM_005118.4:c.*5101T= MANE Select NP_005109.2:n.*5101T=
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