Canonical Allele Identifier: CA2561980262
Gene: TNFSF15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785368T>A , CM000671.2:g.114785368T>A GRCh38
NC_000009.11:g.117547648T>A , CM000671.1:g.117547648T>A GRCh37
NC_000009.10:g.116587469T>A NCBI36
NG_011488.2:g.25761A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5084A>T MANE Select ENSP00000363157.3:n.*5084A>T
ENST00000374045.4:c.*5084A>T ENSP00000363157.3:n.*5084A>T
NM_001204344.1:c.5663A>T NP_001191273.1:n.5663A>T
NM_005118.3:c.*5084A>T NP_005109.2:n.*5084A>T
NM_005118.4:c.*5084A>T MANE Select NP_005109.2:n.*5084A>T
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