Canonical Allele Identifier: CA1111806677
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1801270751
gnomAD v3: 8-23222466-AC-A
gnomAD v4: 8-23222466-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222469del , CM000670.2:g.23222469del GRCh38
NC_000008.10:g.23079982del , CM000670.1:g.23079982del GRCh37
NC_000008.9:g.23135927del NCBI36
NG_032107.1:g.7701del

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2289del MANE Select ENSP00000221132.3:n.306+2289del
ENST00000221132.7:c.306+2289del ENSP00000221132.3:n.306+2289del
ENST00000524158.5:c.-301+1966del ENSP00000428884.1:n.-301+1966del
ENST00000613472.1:c.31+2564del ENSP00000480778.1:n.31+2564del
NM_003844.3:c.306+2289del NP_003835.3:n.306+2289del
NM_003844.4:c.306+2289del MANE Select NP_003835.3:n.306+2289del
Search 100 bp 5'
Search 100 bp 3'