Canonical Allele Identifier: CA2526486448
Gene: TNFSF15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785370_114785371insAGAG , CM000671.2:g.114785370_114785371insAGAG GRCh38
NC_000009.11:g.117547650_117547651insAGAG , CM000671.1:g.117547650_117547651insAGAG GRCh37
NC_000009.10:g.116587471_116587472insAGAG NCBI36
NG_011488.2:g.25758_25759insCTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.*5081_*5082insCTCT MANE Select ENSP00000363157.3:n.*5081_*5082insCTCT
ENST00000374045.4:c.*5081_*5082insCTCT ENSP00000363157.3:n.*5081_*5082insCTCT
NM_001204344.1:c.5660_5661insCTCT NP_001191273.1:n.5660_5661insCTCT
NM_005118.3:c.*5081_*5082insCTCT NP_005109.2:n.*5081_*5082insCTCT
NM_005118.4:c.*5081_*5082insCTCT MANE Select NP_005109.2:n.*5081_*5082insCTCT
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