Canonical Allele Identifier: CA370583079
Gene: TNFRSF10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212115C>T , CM000670.2:g.23212115C>T GRCh38
NC_000008.10:g.23069628C>T , CM000670.1:g.23069628C>T GRCh37
NC_000008.9:g.23125573C>T NCBI36
NG_032107.1:g.18053G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+1G>A MANE Select ENSP00000221132.3:n.403+1G>A
ENST00000221132.7:c.403+1G>A ENSP00000221132.3:n.403+1G>A
ENST00000524158.5:c.-204+1G>A ENSP00000428884.1:n.-204+1G>A
ENST00000613472.1:c.32-9456G>A ENSP00000480778.1:n.32-9456G>A
NM_003844.3:c.403+1G>A NP_003835.3:n.403+1G>A
NM_003844.4:c.403+1G>A MANE Select NP_003835.3:n.403+1G>A