Canonical Allele Identifier: CA1770800807
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222730_23222731delinsGT , CM000670.2:g.23222730_23222731delinsGT GRCh38
NC_000008.10:g.23080243_23080244delinsGT , CM000670.1:g.23080243_23080244delinsGT GRCh37
NC_000008.9:g.23136188_23136189delinsGT NCBI36
NG_032107.1:g.7437_7438delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2025_306+2026delinsAC MANE Select ENSP00000221132.3:n.306+2025_306+2026delinsAC
ENST00000221132.7:c.306+2025_306+2026delinsAC ENSP00000221132.3:n.306+2025_306+2026delinsAC
ENST00000524158.5:c.-301+1702_-301+1703delinsAC ENSP00000428884.1:n.-301+1702_-301+1703delinsAC
ENST00000613472.1:c.31+2300_31+2301delinsAC ENSP00000480778.1:n.31+2300_31+2301delinsAC
NM_003844.3:c.306+2025_306+2026delinsAC NP_003835.3:n.306+2025_306+2026delinsAC
NM_003844.4:c.306+2025_306+2026delinsAC MANE Select NP_003835.3:n.306+2025_306+2026delinsAC
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