Canonical Allele Identifier: CA2587870168

Gene: TNFSF14

Linked Data

• gnomAD v4: 19-6669779-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669780_6669781insGA , CM000681.2:g.6669780_6669781insGA	GRCh38
NC_000019.9:g.6669791_6669792insGA , CM000681.1:g.6669791_6669792insGA	GRCh37
NC_000019.8:g.6620791_6620792insGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.219+71_219+72insCT MANE Select	ENSP00000502837.1:n.219+71_219+72insCT
ENST00000245912.7:c.111+179_111+180insCT	ENSP00000245912.3:n.111+179_111+180insCT
ENST00000599359.1:c.219+71_219+72insCT	ENSP00000469049.1:n.219+71_219+72insCT
NM_003807.3:c.219+71_219+72insCT	NP_003798.2:n.219+71_219+72insCT
NM_172014.2:c.111+179_111+180insCT	NP_742011.2:n.111+179_111+180insCT
XM_005259670.2:c.111+179_111+180insCT	XP_005259727.1:n.111+179_111+180insCT
XM_011528398.1:c.253+37_253+38insCT	XP_011526700.1:n.253+37_253+38insCT
XR_936212.1:n.733+71_733+72insCT
NM_003807.4:c.219+71_219+72insCT	NP_003798.2:n.219+71_219+72insCT
NM_172014.3:c.111+179_111+180insCT	NP_742011.2:n.111+179_111+180insCT
XM_017027417.1:c.219+71_219+72insCT	XP_016882906.1:n.219+71_219+72insCT
XM_017027418.1:c.219+71_219+72insCT	XP_016882907.1:n.219+71_219+72insCT
XR_001753777.1:n.745+71_745+72insCT
XR_936212.2:n.745+71_745+72insCT
NM_001376887.1:c.219+71_219+72insCT MANE Select	NP_001363816.1:n.219+71_219+72insCT
NM_003807.5:c.219+71_219+72insCT	NP_003798.2:n.219+71_219+72insCT