Canonical Allele Identifier: CA580575076
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1181563806
gnomAD v2: 8-23080133-G-GA
gnomAD v3: 8-23222620-G-GA
gnomAD v4: 8-23222620-G-GA
MyVariant Identifiers: chr8:g.23080133_23080134insA (hg19) chr8:g.23222620_23222621insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222621dup , CM000670.2:g.23222621dup GRCh38
NC_000008.10:g.23080134dup , CM000670.1:g.23080134dup GRCh37
NC_000008.9:g.23136079dup NCBI36
NG_032107.1:g.7547dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2135dup MANE Select ENSP00000221132.3:n.306+2135dup
ENST00000221132.7:c.306+2135dup ENSP00000221132.3:n.306+2135dup
ENST00000524158.5:c.-301+1812dup ENSP00000428884.1:n.-301+1812dup
ENST00000613472.1:c.31+2410dup ENSP00000480778.1:n.31+2410dup
NM_003844.3:c.306+2135dup NP_003835.3:n.306+2135dup
NM_003844.4:c.306+2135dup MANE Select NP_003835.3:n.306+2135dup
Search 100 bp 5'
Search 100 bp 3'