Canonical Allele Identifier: CA1770800688

Gene: TNFRSF10A

Linked Data

• dbSNP Id: rs1801270700

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23222461_23222462del , CM000670.2:g.23222461_23222462del	GRCh38
NC_000008.10:g.23079974_23079975del , CM000670.1:g.23079974_23079975del	GRCh37
NC_000008.9:g.23135919_23135920del	NCBI36
NG_032107.1:g.7709_7710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.306+2297_306+2298del MANE Select	ENSP00000221132.3:n.306+2297_306+2298del
ENST00000221132.7:c.306+2297_306+2298del	ENSP00000221132.3:n.306+2297_306+2298del
ENST00000524158.5:c.-301+1974_-301+1975del	ENSP00000428884.1:n.-301+1974_-301+1975del
ENST00000613472.1:c.31+2572_31+2573del	ENSP00000480778.1:n.31+2572_31+2573del
NM_003844.3:c.306+2297_306+2298del	NP_003835.3:n.306+2297_306+2298del
NM_003844.4:c.306+2297_306+2298del MANE Select	NP_003835.3:n.306+2297_306+2298del