Canonical Allele Identifier: CA2686539485
Gene: TNFRSF10A HGNC NCBI

Linked Data

gnomAD v4: 8-23212015-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212019del , CM000670.2:g.23212019del GRCh38
NC_000008.10:g.23069532del , CM000670.1:g.23069532del GRCh37
NC_000008.9:g.23125477del NCBI36
NG_032107.1:g.18152del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+100del MANE Select ENSP00000221132.3:n.403+100del
ENST00000221132.7:c.403+100del ENSP00000221132.3:n.403+100del
ENST00000524158.5:c.-204+100del ENSP00000428884.1:n.-204+100del
ENST00000613472.1:c.32-9357del ENSP00000480778.1:n.32-9357del
NM_003844.3:c.403+100del NP_003835.3:n.403+100del
NM_003844.4:c.403+100del MANE Select NP_003835.3:n.403+100del
Search 100 bp 5'
Search 100 bp 3'