Canonical Allele Identifier: CA2587870106

Gene: TNFSF14

Linked Data

• gnomAD v4: 19-6669755-CACACACACACACACACACAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669763_6669782del , CM000681.2:g.6669763_6669782del	GRCh38
NC_000019.9:g.6669774_6669793del , CM000681.1:g.6669774_6669793del	GRCh37
NC_000019.8:g.6620774_6620793del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.219+76_219+95del MANE Select	ENSP00000502837.1:n.219+76_219+95del
ENST00000245912.7:c.111+184_111+203del	ENSP00000245912.3:n.111+184_111+203del
ENST00000599359.1:c.219+76_219+95del	ENSP00000469049.1:n.219+76_219+95del
NM_003807.3:c.219+76_219+95del	NP_003798.2:n.219+76_219+95del
NM_172014.2:c.111+184_111+203del	NP_742011.2:n.111+184_111+203del
XM_005259670.2:c.111+184_111+203del	XP_005259727.1:n.111+184_111+203del
XM_011528398.1:c.253+42_253+61del	XP_011526700.1:n.253+42_253+61del
XR_936212.1:n.733+76_733+95del
NM_003807.4:c.219+76_219+95del	NP_003798.2:n.219+76_219+95del
NM_172014.3:c.111+184_111+203del	NP_742011.2:n.111+184_111+203del
XM_017027417.1:c.219+76_219+95del	XP_016882906.1:n.219+76_219+95del
XM_017027418.1:c.219+76_219+95del	XP_016882907.1:n.219+76_219+95del
XR_001753777.1:n.745+76_745+95del
XR_936212.2:n.745+76_745+95del
NM_001376887.1:c.219+76_219+95del MANE Select	NP_001363816.1:n.219+76_219+95del
NM_003807.5:c.219+76_219+95del	NP_003798.2:n.219+76_219+95del