Canonical Allele Identifier: CA2587870179

Gene: TNFSF14

Linked Data

• gnomAD v4: 19-6669787-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669787C>A , CM000681.2:g.6669787C>A	GRCh38
NC_000019.9:g.6669798C>A , CM000681.1:g.6669798C>A	GRCh37
NC_000019.8:g.6620798C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675206.1:c.219+64G>T MANE Select	ENSP00000502837.1:n.219+64G>T
ENST00000245912.7:c.111+172G>T	ENSP00000245912.3:n.111+172G>T
ENST00000599359.1:c.219+64G>T	ENSP00000469049.1:n.219+64G>T
NM_003807.3:c.219+64G>T	NP_003798.2:n.219+64G>T
NM_172014.2:c.111+172G>T	NP_742011.2:n.111+172G>T
XM_005259670.2:c.111+172G>T	XP_005259727.1:n.111+172G>T
XM_011528398.1:c.253+30G>T	XP_011526700.1:n.253+30G>T
XR_936212.1:n.733+64G>T
NM_003807.4:c.219+64G>T	NP_003798.2:n.219+64G>T
NM_172014.3:c.111+172G>T	NP_742011.2:n.111+172G>T
XM_017027417.1:c.219+64G>T	XP_016882906.1:n.219+64G>T
XM_017027418.1:c.219+64G>T	XP_016882907.1:n.219+64G>T
XR_001753777.1:n.745+64G>T
XR_936212.2:n.745+64G>T
NM_001376887.1:c.219+64G>T MANE Select	NP_001363816.1:n.219+64G>T
NM_003807.5:c.219+64G>T	NP_003798.2:n.219+64G>T