Canonical Allele Identifier: CA1770800800
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222709T= , CM000670.2:g.23222709T= GRCh38
NC_000008.10:g.23080222T= , CM000670.1:g.23080222T= GRCh37
NC_000008.9:g.23136167T= NCBI36
NG_032107.1:g.7459A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2047A= MANE Select ENSP00000221132.3:n.306+2047A=
ENST00000221132.7:c.306+2047A= ENSP00000221132.3:n.306+2047A=
ENST00000524158.5:c.-301+1724A= ENSP00000428884.1:n.-301+1724A=
ENST00000613472.1:c.31+2322A= ENSP00000480778.1:n.31+2322A=
NM_003844.3:c.306+2047A= NP_003835.3:n.306+2047A=
NM_003844.4:c.306+2047A= MANE Select NP_003835.3:n.306+2047A=
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