Canonical Allele Identifier: CA1770800698

Gene: TNFRSF10A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23222477_23222480delinsAAAT , CM000670.2:g.23222477_23222480delinsAAAT	GRCh38
NC_000008.10:g.23079990_23079993delinsAAAT , CM000670.1:g.23079990_23079993delinsAAAT	GRCh37
NC_000008.9:g.23135935_23135938delinsAAAT	NCBI36
NG_032107.1:g.7688_7691delinsATTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000221132.8:c.306+2276_306+2279delinsATTT MANE Select	ENSP00000221132.3:n.306+2276_306+2279delinsATTT
ENST00000221132.7:c.306+2276_306+2279delinsATTT	ENSP00000221132.3:n.306+2276_306+2279delinsATTT
ENST00000524158.5:c.-301+1953_-301+1956delinsATTT	ENSP00000428884.1:n.-301+1953_-301+1956delinsATTT
ENST00000613472.1:c.31+2551_31+2554delinsATTT	ENSP00000480778.1:n.31+2551_31+2554delinsATTT
NM_003844.3:c.306+2276_306+2279delinsATTT	NP_003835.3:n.306+2276_306+2279delinsATTT
NM_003844.4:c.306+2276_306+2279delinsATTT MANE Select	NP_003835.3:n.306+2276_306+2279delinsATTT