Canonical Allele Identifier: CA918220090
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1585289947

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222466dup , CM000670.2:g.23222466dup GRCh38
NC_000008.10:g.23079979dup , CM000670.1:g.23079979dup GRCh37
NC_000008.9:g.23135924dup NCBI36
NG_032107.1:g.7702dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2290dup MANE Select ENSP00000221132.3:n.306+2290dup
ENST00000221132.7:c.306+2290dup ENSP00000221132.3:n.306+2290dup
ENST00000524158.5:c.-301+1967dup ENSP00000428884.1:n.-301+1967dup
ENST00000613472.1:c.31+2565dup ENSP00000480778.1:n.31+2565dup
NM_003844.3:c.306+2290dup NP_003835.3:n.306+2290dup
NM_003844.4:c.306+2290dup MANE Select NP_003835.3:n.306+2290dup