Canonical Allele Identifier: CA1770800759
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1801272479

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222644G>A , CM000670.2:g.23222644G>A GRCh38
NC_000008.10:g.23080157G>A , CM000670.1:g.23080157G>A GRCh37
NC_000008.9:g.23136102G>A NCBI36
NG_032107.1:g.7524C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2112C>T MANE Select ENSP00000221132.3:n.306+2112C>T
ENST00000221132.7:c.306+2112C>T ENSP00000221132.3:n.306+2112C>T
ENST00000524158.5:c.-301+1789C>T ENSP00000428884.1:n.-301+1789C>T
ENST00000613472.1:c.31+2387C>T ENSP00000480778.1:n.31+2387C>T
NM_003844.3:c.306+2112C>T NP_003835.3:n.306+2112C>T
NM_003844.4:c.306+2112C>T MANE Select NP_003835.3:n.306+2112C>T