Canonical Allele Identifier: CA1770800694
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222470A= , CM000670.2:g.23222470A= GRCh38
NC_000008.10:g.23079983A= , CM000670.1:g.23079983A= GRCh37
NC_000008.9:g.23135928A= NCBI36
NG_032107.1:g.7698T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2286T= MANE Select ENSP00000221132.3:n.306+2286T=
ENST00000221132.7:c.306+2286T= ENSP00000221132.3:n.306+2286T=
ENST00000524158.5:c.-301+1963T= ENSP00000428884.1:n.-301+1963T=
ENST00000613472.1:c.31+2561T= ENSP00000480778.1:n.31+2561T=
NM_003844.3:c.306+2286T= NP_003835.3:n.306+2286T=
NM_003844.4:c.306+2286T= MANE Select NP_003835.3:n.306+2286T=