Canonical Allele Identifier: CA1770754260
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191835_23191837delinsGTT , CM000670.2:g.23191835_23191837delinsGTT GRCh38
NC_000008.10:g.23049348_23049350delinsGTT , CM000670.1:g.23049348_23049350delinsGTT GRCh37
NC_000008.9:g.23105293_23105295delinsGTT NCBI36
NG_032107.1:g.38331_38333delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1264_1266delinsAAC MANE Select ENSP00000221132.3:p.Asn422=
ENST00000221132.7:c.1264_1266delinsAAC ENSP00000221132.3:p.Asn422=
ENST00000519862.1:n.319_321delinsAAC
ENST00000613472.1:c.790_792delinsAAC ENSP00000480778.1:p.Asn264=
NM_003844.3:c.1264_1266delinsAAC NP_003835.3:p.Asn422=
NM_003844.4:c.1264_1266delinsAAC MANE Select NP_003835.3:p.Asn422=
Search 100 bp 5'
Search 100 bp 3'