Canonical Allele Identifier: CA1770800686

Gene: TNFRSF10A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23222457_23222459delinsATG , CM000670.2:g.23222457_23222459delinsATG	GRCh38
NC_000008.10:g.23079970_23079972delinsATG , CM000670.1:g.23079970_23079972delinsATG	GRCh37
NC_000008.9:g.23135915_23135917delinsATG	NCBI36
NG_032107.1:g.7709_7711delinsCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000221132.8:c.306+2297_306+2299delinsCAT MANE Select	ENSP00000221132.3:n.306+2297_306+2299delinsCAT
ENST00000221132.7:c.306+2297_306+2299delinsCAT	ENSP00000221132.3:n.306+2297_306+2299delinsCAT
ENST00000524158.5:c.-301+1974_-301+1976delinsCAT	ENSP00000428884.1:n.-301+1974_-301+1976delinsCAT
ENST00000613472.1:c.31+2572_31+2574delinsCAT	ENSP00000480778.1:n.31+2572_31+2574delinsCAT
NM_003844.3:c.306+2297_306+2299delinsCAT	NP_003835.3:n.306+2297_306+2299delinsCAT
NM_003844.4:c.306+2297_306+2299delinsCAT MANE Select	NP_003835.3:n.306+2297_306+2299delinsCAT