Canonical Allele Identifier: CA1874003168
Gene: TNFSF15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785441G= , CM000671.2:g.114785441G= GRCh38
NC_000009.11:g.117547721G= , CM000671.1:g.117547721G= GRCh37
NC_000009.10:g.116587542G= NCBI36
NG_011488.2:g.25688C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.*5011C= MANE Select ENSP00000363157.3:n.*5011C=
ENST00000374045.4:c.*5011C= ENSP00000363157.3:n.*5011C=
NM_001204344.1:c.5590C= NP_001191273.1:n.5590C=
NM_005118.3:c.*5011C= NP_005109.2:n.*5011C=
NM_005118.4:c.*5011C= MANE Select NP_005109.2:n.*5011C=
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