Canonical Allele Identifier: CA1770800749

Gene: TNFRSF10A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23222617_23222619delinsTGA , CM000670.2:g.23222617_23222619delinsTGA	GRCh38
NC_000008.10:g.23080130_23080132delinsTGA , CM000670.1:g.23080130_23080132delinsTGA	GRCh37
NC_000008.9:g.23136075_23136077delinsTGA	NCBI36
NG_032107.1:g.7549_7551delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.306+2137_306+2139delinsTCA MANE Select	ENSP00000221132.3:n.306+2137_306+2139delinsTCA
ENST00000221132.7:c.306+2137_306+2139delinsTCA	ENSP00000221132.3:n.306+2137_306+2139delinsTCA
ENST00000524158.5:c.-301+1814_-301+1816delinsTCA	ENSP00000428884.1:n.-301+1814_-301+1816delinsTCA
ENST00000613472.1:c.31+2412_31+2414delinsTCA	ENSP00000480778.1:n.31+2412_31+2414delinsTCA
NM_003844.3:c.306+2137_306+2139delinsTCA	NP_003835.3:n.306+2137_306+2139delinsTCA
NM_003844.4:c.306+2137_306+2139delinsTCA MANE Select	NP_003835.3:n.306+2137_306+2139delinsTCA