Canonical Allele Identifier: CA1770800695

Gene: TNFRSF10A

Linked Data

• dbSNP Id: rs1801270828

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23222470A>C , CM000670.2:g.23222470A>C	GRCh38
NC_000008.10:g.23079983A>C , CM000670.1:g.23079983A>C	GRCh37
NC_000008.9:g.23135928A>C	NCBI36
NG_032107.1:g.7698T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000221132.8:c.306+2286T>G MANE Select	ENSP00000221132.3:n.306+2286T>G
ENST00000221132.7:c.306+2286T>G	ENSP00000221132.3:n.306+2286T>G
ENST00000524158.5:c.-301+1963T>G	ENSP00000428884.1:n.-301+1963T>G
ENST00000613472.1:c.31+2561T>G	ENSP00000480778.1:n.31+2561T>G
NM_003844.3:c.306+2286T>G	NP_003835.3:n.306+2286T>G
NM_003844.4:c.306+2286T>G MANE Select	NP_003835.3:n.306+2286T>G