Canonical Allele Identifier: CA2320545693
Gene: TNFSF14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6669881C= , CM000681.2:g.6669881C= GRCh38
NC_000019.9:g.6669892C= , CM000681.1:g.6669892C= GRCh37
NC_000019.8:g.6620892C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000675206.1:c.189G= MANE Select ENSP00000502837.1:p.Trp63=
ENST00000245912.7:c.111+78G= ENSP00000245912.3:n.111+78G=
ENST00000599359.1:c.189G= ENSP00000469049.1:p.Trp63=
NM_003807.3:c.189G= NP_003798.2:p.Trp63=
NM_172014.2:c.111+78G= NP_742011.2:n.111+78G=
XM_005259670.2:c.111+78G= XP_005259727.1:n.111+78G=
XM_011528398.1:c.189G= XP_011526700.1:p.Trp63=
XR_936212.1:n.703G=
NM_003807.4:c.189G= NP_003798.2:p.Trp63=
NM_172014.3:c.111+78G= NP_742011.2:n.111+78G=
XM_017027417.1:c.189G= XP_016882906.1:p.Trp63=
XM_017027418.1:c.189G= XP_016882907.1:p.Trp63=
XR_001753777.1:n.715G=
XR_936212.2:n.715G=
NM_001376887.1:c.189G= MANE Select NP_001363816.1:p.Trp63=
NM_003807.5:c.189G= NP_003798.2:p.Trp63=