Canonical Allele Identifier: CA2691385591

Gene: TNFSF15

Linked Data

• gnomAD v4: 9-114785313-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114785313G>A , CM000671.2:g.114785313G>A	GRCh38
NC_000009.11:g.117547593G>A , CM000671.1:g.117547593G>A	GRCh37
NC_000009.10:g.116587414G>A	NCBI36
NG_011488.2:g.25816C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374045.5:c.*5139C>T MANE Select	ENSP00000363157.3:n.*5139C>T
ENST00000374045.4:c.*5139C>T	ENSP00000363157.3:n.*5139C>T
NM_001204344.1:c.5718C>T	NP_001191273.1:n.5718C>T
NM_005118.3:c.*5139C>T	NP_005109.2:n.*5139C>T
NM_005118.4:c.*5139C>T MANE Select	NP_005109.2:n.*5139C>T