Canonical Allele Identifier: CA403626949

Gene: TNFSF14

Linked Data

• MyVariant Identifiers: chr19:g.6669891G>T (hg19) ; chr19:g.6669880G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669880G>T , CM000681.2:g.6669880G>T	GRCh38
NC_000019.9:g.6669891G>T , CM000681.1:g.6669891G>T	GRCh37
NC_000019.8:g.6620891G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.190C>A MANE Select	ENSP00000502837.1:p.Arg64Ser
ENST00000245912.7:c.111+79C>A	ENSP00000245912.3:n.111+79C>A
ENST00000599359.1:c.190C>A	ENSP00000469049.1:p.Arg64Ser
NM_003807.3:c.190C>A	NP_003798.2:p.Arg64Ser
NM_172014.2:c.111+79C>A	NP_742011.2:n.111+79C>A
XM_005259670.2:c.111+79C>A	XP_005259727.1:n.111+79C>A
XM_011528398.1:c.190C>A	XP_011526700.1:p.Arg64Ser
XR_936212.1:n.704C>A
NM_003807.4:c.190C>A	NP_003798.2:p.Arg64Ser
NM_172014.3:c.111+79C>A	NP_742011.2:n.111+79C>A
XM_017027417.1:c.190C>A	XP_016882906.1:p.Arg64Ser
XM_017027418.1:c.190C>A	XP_016882907.1:p.Arg64Ser
XR_001753777.1:n.716C>A
XR_936212.2:n.716C>A
NM_001376887.1:c.190C>A MANE Select	NP_001363816.1:p.Arg64Ser
NM_003807.5:c.190C>A	NP_003798.2:p.Arg64Ser