Canonical Allele Identifier: CA505117984

Gene: TNFSF14

Linked Data

• MyVariant Identifiers: chr19:g.6670003T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669992T>G , CM000681.2:g.6669992T>G	GRCh38
NC_000019.9:g.6670003T>G , CM000681.1:g.6670003T>G	GRCh37
NC_000019.8:g.6621003T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675206.1:c.78A>C MANE Select	ENSP00000502837.1:p.Arg26=
ENST00000245912.7:c.78A>C	ENSP00000245912.3:p.Arg26=
ENST00000599359.1:c.78A>C	ENSP00000469049.1:p.Arg26=
NM_003807.3:c.78A>C	NP_003798.2:p.Arg26=
NM_172014.2:c.78A>C	NP_742011.2:p.Arg26=
XM_005259670.2:c.78A>C	XP_005259727.1:p.Arg26=
XM_011528398.1:c.78A>C	XP_011526700.1:p.Arg26=
XR_936212.1:n.592A>C
NM_003807.4:c.78A>C	NP_003798.2:p.Arg26=
NM_172014.3:c.78A>C	NP_742011.2:p.Arg26=
XM_017027417.1:c.78A>C	XP_016882906.1:p.Arg26=
XM_017027418.1:c.78A>C	XP_016882907.1:p.Arg26=
XR_001753777.1:n.604A>C
XR_936212.2:n.604A>C
NM_001376887.1:c.78A>C MANE Select	NP_001363816.1:p.Arg26=
NM_003807.5:c.78A>C	NP_003798.2:p.Arg26=