Canonical Allele Identifier: CA1770754058
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191778_23191779delinsTC , CM000670.2:g.23191778_23191779delinsTC GRCh38
NC_000008.10:g.23049291_23049292delinsTC , CM000670.1:g.23049291_23049292delinsTC GRCh37
NC_000008.9:g.23105236_23105237delinsTC NCBI36
NG_032107.1:g.38389_38390delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1322_1323delinsGA MANE Select ENSP00000221132.3:p.Arg441=
ENST00000221132.7:c.1322_1323delinsGA ENSP00000221132.3:p.Arg441=
ENST00000613472.1:c.848_849delinsGA ENSP00000480778.1:p.Arg283=
NM_003844.3:c.1322_1323delinsGA NP_003835.3:p.Arg441=
NM_003844.4:c.1322_1323delinsGA MANE Select NP_003835.3:p.Arg441=
Search 100 bp 5'
Search 100 bp 3'