Canonical Allele Identifier: CA2779393490
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212093del , CM000670.2:g.23212093del GRCh38
NC_000008.10:g.23069606del , CM000670.1:g.23069606del GRCh37
NC_000008.9:g.23125551del NCBI36
NG_032107.1:g.18076del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+24del MANE Select ENSP00000221132.3:n.403+24del
ENST00000221132.7:c.403+24del ENSP00000221132.3:n.403+24del
ENST00000524158.5:c.-204+24del ENSP00000428884.1:n.-204+24del
ENST00000613472.1:c.32-9433del ENSP00000480778.1:n.32-9433del
NM_003844.3:c.403+24del NP_003835.3:n.403+24del
NM_003844.4:c.403+24del MANE Select NP_003835.3:n.403+24del