Canonical Allele Identifier: CA2779393042
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222527A>G , CM000670.2:g.23222527A>G GRCh38
NC_000008.10:g.23080040A>G , CM000670.1:g.23080040A>G GRCh37
NC_000008.9:g.23135985A>G NCBI36
NG_032107.1:g.7641T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2229T>C MANE Select ENSP00000221132.3:n.306+2229T>C
ENST00000221132.7:c.306+2229T>C ENSP00000221132.3:n.306+2229T>C
ENST00000524158.5:c.-301+1906T>C ENSP00000428884.1:n.-301+1906T>C
ENST00000613472.1:c.31+2504T>C ENSP00000480778.1:n.31+2504T>C
NM_003844.3:c.306+2229T>C NP_003835.3:n.306+2229T>C
NM_003844.4:c.306+2229T>C MANE Select NP_003835.3:n.306+2229T>C