Canonical Allele Identifier: CA1770756326
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1801101906
gnomAD v4: 8-23212190-GTTGCAGCTGAGCTAGGTA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212191_23212208del , CM000670.2:g.23212191_23212208del GRCh38
NC_000008.10:g.23069704_23069721del , CM000670.1:g.23069704_23069721del GRCh37
NC_000008.9:g.23125649_23125666del NCBI36
NG_032107.1:g.17960_17977del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.311_328del MANE Select ENSP00000221132.3:p.Val104_Thr110delinsAla
ENST00000221132.7:c.311_328del ENSP00000221132.3:p.Val104_Thr110delinsAla
ENST00000524158.5:c.-296_-279del ENSP00000428884.1:n.-296_-279del
ENST00000613472.1:c.32-9549_32-9532del ENSP00000480778.1:n.32-9549_32-9532del
NM_003844.3:c.311_328del NP_003835.3:p.Val104_Thr110delinsAla
NM_003844.4:c.311_328del MANE Select NP_003835.3:p.Val104_Thr110delinsAla
Search 100 bp 5'
Search 100 bp 3'