Canonical Allele Identifier: CA370568681
Gene: TNFRSF10A HGNC NCBI

Linked Data

gnomAD v4: 8-23191816-G-C
MyVariant Identifiers: chr8:g.23049329G>C (hg19) chr8:g.23191816G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191816G>C , CM000670.2:g.23191816G>C GRCh38
NC_000008.10:g.23049329G>C , CM000670.1:g.23049329G>C GRCh37
NC_000008.9:g.23105274G>C NCBI36
NG_032107.1:g.38352C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1285C>G MANE Select ENSP00000221132.3:p.Leu429Val
ENST00000221132.7:c.1285C>G ENSP00000221132.3:p.Leu429Val
ENST00000519862.1:n.340C>G
ENST00000613472.1:c.811C>G ENSP00000480778.1:p.Leu271Val
NM_003844.3:c.1285C>G NP_003835.3:p.Leu429Val
NM_003844.4:c.1285C>G MANE Select NP_003835.3:p.Leu429Val
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