Canonical Allele Identifier: CA1770800801
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222715G= , CM000670.2:g.23222715G= GRCh38
NC_000008.10:g.23080228G= , CM000670.1:g.23080228G= GRCh37
NC_000008.9:g.23136173G= NCBI36
NG_032107.1:g.7453C=

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2041C= MANE Select ENSP00000221132.3:n.306+2041C=
ENST00000221132.7:c.306+2041C= ENSP00000221132.3:n.306+2041C=
ENST00000524158.5:c.-301+1718C= ENSP00000428884.1:n.-301+1718C=
ENST00000613472.1:c.31+2316C= ENSP00000480778.1:n.31+2316C=
NM_003844.3:c.306+2041C= NP_003835.3:n.306+2041C=
NM_003844.4:c.306+2041C= MANE Select NP_003835.3:n.306+2041C=
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