Canonical Allele Identifier: CA2320545695
Gene: TNFSF14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6669885T= , CM000681.2:g.6669885T= GRCh38
NC_000019.9:g.6669896T= , CM000681.1:g.6669896T= GRCh37
NC_000019.8:g.6620896T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000675206.1:c.185A= MANE Select ENSP00000502837.1:p.His62=
ENST00000245912.7:c.111+74A= ENSP00000245912.3:n.111+74A=
ENST00000599359.1:c.185A= ENSP00000469049.1:p.His62=
NM_003807.3:c.185A= NP_003798.2:p.His62=
NM_172014.2:c.111+74A= NP_742011.2:n.111+74A=
XM_005259670.2:c.111+74A= XP_005259727.1:n.111+74A=
XM_011528398.1:c.185A= XP_011526700.1:p.His62=
XR_936212.1:n.699A=
NM_003807.4:c.185A= NP_003798.2:p.His62=
NM_172014.3:c.111+74A= NP_742011.2:n.111+74A=
XM_017027417.1:c.185A= XP_016882906.1:p.His62=
XM_017027418.1:c.185A= XP_016882907.1:p.His62=
XR_001753777.1:n.711A=
XR_936212.2:n.711A=
NM_001376887.1:c.185A= MANE Select NP_001363816.1:p.His62=
NM_003807.5:c.185A= NP_003798.2:p.His62=