Canonical Allele Identifier: CA1770754357
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191857C= , CM000670.2:g.23191857C= GRCh38
NC_000008.10:g.23049370C= , CM000670.1:g.23049370C= GRCh37
NC_000008.9:g.23105315C= NCBI36
NG_032107.1:g.38311G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1244G= MANE Select ENSP00000221132.3:p.Trp415=
ENST00000221132.7:c.1244G= ENSP00000221132.3:p.Trp415=
ENST00000519862.1:n.299G=
ENST00000613472.1:c.770G= ENSP00000480778.1:p.Trp257=
NM_003844.3:c.1244G= NP_003835.3:p.Trp415=
NM_003844.4:c.1244G= MANE Select NP_003835.3:p.Trp415=