Canonical Allele Identifier: CA1770800798
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222707T= , CM000670.2:g.23222707T= GRCh38
NC_000008.10:g.23080220T= , CM000670.1:g.23080220T= GRCh37
NC_000008.9:g.23136165T= NCBI36
NG_032107.1:g.7461A=

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2049A= MANE Select ENSP00000221132.3:n.306+2049A=
ENST00000221132.7:c.306+2049A= ENSP00000221132.3:n.306+2049A=
ENST00000524158.5:c.-301+1726A= ENSP00000428884.1:n.-301+1726A=
ENST00000613472.1:c.31+2324A= ENSP00000480778.1:n.31+2324A=
NM_003844.3:c.306+2049A= NP_003835.3:n.306+2049A=
NM_003844.4:c.306+2049A= MANE Select NP_003835.3:n.306+2049A=
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