Canonical Allele Identifier: CA993057354

Gene: TNFSF14

Linked Data

• gnomAD v3: 19-6669782-AGTGACC-A
• gnomAD v4: 19-6669782-AGTGACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669783_6669788del , CM000681.2:g.6669783_6669788del	GRCh38
NC_000019.9:g.6669794_6669799del , CM000681.1:g.6669794_6669799del	GRCh37
NC_000019.8:g.6620794_6620799del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.219+63_219+68del MANE Select	ENSP00000502837.1:n.219+63_219+68del
ENST00000245912.7:c.111+171_111+176del	ENSP00000245912.3:n.111+171_111+176del
ENST00000599359.1:c.219+63_219+68del	ENSP00000469049.1:n.219+63_219+68del
NM_003807.3:c.219+63_219+68del	NP_003798.2:n.219+63_219+68del
NM_172014.2:c.111+171_111+176del	NP_742011.2:n.111+171_111+176del
XM_005259670.2:c.111+171_111+176del	XP_005259727.1:n.111+171_111+176del
XM_011528398.1:c.253+29_253+34del	XP_011526700.1:n.253+29_253+34del
XR_936212.1:n.733+63_733+68del
NM_003807.4:c.219+63_219+68del	NP_003798.2:n.219+63_219+68del
NM_172014.3:c.111+171_111+176del	NP_742011.2:n.111+171_111+176del
XM_017027417.1:c.219+63_219+68del	XP_016882906.1:n.219+63_219+68del
XM_017027418.1:c.219+63_219+68del	XP_016882907.1:n.219+63_219+68del
XR_001753777.1:n.745+63_745+68del
XR_936212.2:n.745+63_745+68del
NM_001376887.1:c.219+63_219+68del MANE Select	NP_001363816.1:n.219+63_219+68del
NM_003807.5:c.219+63_219+68del	NP_003798.2:n.219+63_219+68del