Canonical Allele Identifier: CA1770800710
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1585289964

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222501A>G , CM000670.2:g.23222501A>G GRCh38
NC_000008.10:g.23080014A>G , CM000670.1:g.23080014A>G GRCh37
NC_000008.9:g.23135959A>G NCBI36
NG_032107.1:g.7667T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2255T>C MANE Select ENSP00000221132.3:n.306+2255T>C
ENST00000221132.7:c.306+2255T>C ENSP00000221132.3:n.306+2255T>C
ENST00000524158.5:c.-301+1932T>C ENSP00000428884.1:n.-301+1932T>C
ENST00000613472.1:c.31+2530T>C ENSP00000480778.1:n.31+2530T>C
NM_003844.3:c.306+2255T>C NP_003835.3:n.306+2255T>C
NM_003844.4:c.306+2255T>C MANE Select NP_003835.3:n.306+2255T>C