Canonical Allele Identifier: CA884158137

Gene: TNFSF14

Linked Data

• dbSNP Id: rs1320933172
• gnomAD v4: 19-6669771-CACAG-C
• MyVariant Identifiers: chr19:g.6669783_6669786del (hg19) ; chr19:g.6669772_6669775del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669775_6669778del , CM000681.2:g.6669775_6669778del	GRCh38
NC_000019.9:g.6669786_6669789del , CM000681.1:g.6669786_6669789del	GRCh37
NC_000019.8:g.6620786_6620789del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.219+76_219+79del MANE Select	ENSP00000502837.1:n.219+76_219+79del
ENST00000245912.7:c.111+184_111+187del	ENSP00000245912.3:n.111+184_111+187del
ENST00000599359.1:c.219+76_219+79del	ENSP00000469049.1:n.219+76_219+79del
NM_003807.3:c.219+76_219+79del	NP_003798.2:n.219+76_219+79del
NM_172014.2:c.111+184_111+187del	NP_742011.2:n.111+184_111+187del
XM_005259670.2:c.111+184_111+187del	XP_005259727.1:n.111+184_111+187del
XM_011528398.1:c.253+42_253+45del	XP_011526700.1:n.253+42_253+45del
XR_936212.1:n.733+76_733+79del
NM_003807.4:c.219+76_219+79del	NP_003798.2:n.219+76_219+79del
NM_172014.3:c.111+184_111+187del	NP_742011.2:n.111+184_111+187del
XM_017027417.1:c.219+76_219+79del	XP_016882906.1:n.219+76_219+79del
XM_017027418.1:c.219+76_219+79del	XP_016882907.1:n.219+76_219+79del
XR_001753777.1:n.745+76_745+79del
XR_936212.2:n.745+76_745+79del
NM_001376887.1:c.219+76_219+79del MANE Select	NP_001363816.1:n.219+76_219+79del
NM_003807.5:c.219+76_219+79del	NP_003798.2:n.219+76_219+79del