Canonical Allele Identifier: CA1770800777
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222672C= , CM000670.2:g.23222672C= GRCh38
NC_000008.10:g.23080185C= , CM000670.1:g.23080185C= GRCh37
NC_000008.9:g.23136130C= NCBI36
NG_032107.1:g.7496G=

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2084G= MANE Select ENSP00000221132.3:n.306+2084G=
ENST00000221132.7:c.306+2084G= ENSP00000221132.3:n.306+2084G=
ENST00000524158.5:c.-301+1761G= ENSP00000428884.1:n.-301+1761G=
ENST00000613472.1:c.31+2359G= ENSP00000480778.1:n.31+2359G=
NM_003844.3:c.306+2084G= NP_003835.3:n.306+2084G=
NM_003844.4:c.306+2084G= MANE Select NP_003835.3:n.306+2084G=