Canonical Allele Identifier: CA505118360

Gene: TNFSF14

Linked Data

• gnomAD v4: 19-6670051-G-T
• MyVariant Identifiers: chr19:g.6670062G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6670051G>T , CM000681.2:g.6670051G>T	GRCh38
NC_000019.9:g.6670062G>T , CM000681.1:g.6670062G>T	GRCh37
NC_000019.8:g.6621062G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675206.1:c.19C>A MANE Select	ENSP00000502837.1:p.Arg7=
ENST00000245912.7:c.19C>A	ENSP00000245912.3:p.Arg7=
ENST00000599359.1:c.19C>A	ENSP00000469049.1:p.Arg7=
NM_003807.3:c.19C>A	NP_003798.2:p.Arg7=
NM_172014.2:c.19C>A	NP_742011.2:p.Arg7=
XM_005259670.2:c.19C>A	XP_005259727.1:p.Arg7=
XM_011528398.1:c.19C>A	XP_011526700.1:p.Arg7=
XR_936212.1:n.533C>A
NM_003807.4:c.19C>A	NP_003798.2:p.Arg7=
NM_172014.3:c.19C>A	NP_742011.2:p.Arg7=
XM_017027417.1:c.19C>A	XP_016882906.1:p.Arg7=
XM_017027418.1:c.19C>A	XP_016882907.1:p.Arg7=
XR_001753777.1:n.545C>A
XR_936212.2:n.545C>A
NM_001376887.1:c.19C>A MANE Select	NP_001363816.1:p.Arg7=
NM_003807.5:c.19C>A	NP_003798.2:p.Arg7=