Canonical Allele Identifier: CA1770800690
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222465C= , CM000670.2:g.23222465C= GRCh38
NC_000008.10:g.23079978C= , CM000670.1:g.23079978C= GRCh37
NC_000008.9:g.23135923C= NCBI36
NG_032107.1:g.7703G=

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2291G= MANE Select ENSP00000221132.3:n.306+2291G=
ENST00000221132.7:c.306+2291G= ENSP00000221132.3:n.306+2291G=
ENST00000524158.5:c.-301+1968G= ENSP00000428884.1:n.-301+1968G=
ENST00000613472.1:c.31+2566G= ENSP00000480778.1:n.31+2566G=
NM_003844.3:c.306+2291G= NP_003835.3:n.306+2291G=
NM_003844.4:c.306+2291G= MANE Select NP_003835.3:n.306+2291G=
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