Canonical Allele Identifier: CA1770800779
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222676G= , CM000670.2:g.23222676G= GRCh38
NC_000008.10:g.23080189G= , CM000670.1:g.23080189G= GRCh37
NC_000008.9:g.23136134G= NCBI36
NG_032107.1:g.7492C=

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2080C= MANE Select ENSP00000221132.3:n.306+2080C=
ENST00000221132.7:c.306+2080C= ENSP00000221132.3:n.306+2080C=
ENST00000524158.5:c.-301+1757C= ENSP00000428884.1:n.-301+1757C=
ENST00000613472.1:c.31+2355C= ENSP00000480778.1:n.31+2355C=
NM_003844.3:c.306+2080C= NP_003835.3:n.306+2080C=
NM_003844.4:c.306+2080C= MANE Select NP_003835.3:n.306+2080C=