Canonical Allele Identifier: CA2524999011
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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