Canonical Allele Identifier: CA370569190
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23049391A>C (hg19) chr8:g.23191878A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191878A>C , CM000670.2:g.23191878A>C GRCh38
NC_000008.10:g.23049391A>C , CM000670.1:g.23049391A>C GRCh37
NC_000008.9:g.23105336A>C NCBI36
NG_032107.1:g.38290T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1223T>G MANE Select ENSP00000221132.3:p.Leu408Trp
ENST00000221132.7:c.1223T>G ENSP00000221132.3:p.Leu408Trp
ENST00000519862.1:n.278T>G
ENST00000613472.1:c.749T>G ENSP00000480778.1:p.Leu250Trp
NM_003844.3:c.1223T>G NP_003835.3:p.Leu408Trp
NM_003844.4:c.1223T>G MANE Select NP_003835.3:p.Leu408Trp
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