Canonical Allele Identifier: CA1770754182
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191819G= , CM000670.2:g.23191819G= GRCh38
NC_000008.10:g.23049332G= , CM000670.1:g.23049332G= GRCh37
NC_000008.9:g.23105277G= NCBI36
NG_032107.1:g.38349C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1282C= MANE Select ENSP00000221132.3:p.Leu428=
ENST00000221132.7:c.1282C= ENSP00000221132.3:p.Leu428=
ENST00000519862.1:n.337C=
ENST00000613472.1:c.808C= ENSP00000480778.1:p.Leu270=
NM_003844.3:c.1282C= NP_003835.3:p.Leu428=
NM_003844.4:c.1282C= MANE Select NP_003835.3:p.Leu428=