Canonical Allele Identifier: CA580575073

Gene: TNFRSF10A

Linked Data

• gnomAD v2: 8-23080021-T-TACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGC
• MyVariant Identifiers: chr8:g.23080021_23080022insACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGC (hg19) ; chr8:g.23222508_23222509insACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23222510_23222511insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC , CM000670.2:g.23222510_23222511insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	GRCh38
NC_000008.10:g.23080023_23080024insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC , CM000670.1:g.23080023_23080024insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	GRCh37
NC_000008.9:g.23135968_23135969insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	NCBI36
NG_032107.1:g.7659_7660insGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000221132.8:c.306+2247_306+2248insGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGT MANE Select	ENSP00000221132.3:n.306+2247_306+2248insGCTGGGATTACAGGCGTGAGC...
ENST00000221132.7:c.306+2247_306+2248insGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGT	ENSP00000221132.3:n.306+2247_306+2248insGCTGGGATTACAGGCGTGAGC...
ENST00000524158.5:c.-301+1924_-301+1925insGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGT	ENSP00000428884.1:n.-301+1924_-301+1925insGCTGGGATTACAGGCGTGA...
ENST00000613472.1:c.31+2522_31+2523insGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGT	ENSP00000480778.1:n.31+2522_31+2523insGCTGGGATTACAGGCGTGAGCCA...
NM_003844.3:c.306+2247_306+2248insGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGT	NP_003835.3:n.306+2247_306+2248insGCTGGGATTACAGGCGTGAGCCACCGC...
NM_003844.4:c.306+2247_306+2248insGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGT MANE Select	NP_003835.3:n.306+2247_306+2248insGCTGGGATTACAGGCGTGAGCCACCGC...