Canonical Allele Identifier: CA2686539549
Gene: TNFRSF10A HGNC NCBI

Linked Data

gnomAD v4: 8-23212108-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212108G>A , CM000670.2:g.23212108G>A GRCh38
NC_000008.10:g.23069621G>A , CM000670.1:g.23069621G>A GRCh37
NC_000008.9:g.23125566G>A NCBI36
NG_032107.1:g.18060C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+8C>T MANE Select ENSP00000221132.3:n.403+8C>T
ENST00000221132.7:c.403+8C>T ENSP00000221132.3:n.403+8C>T
ENST00000524158.5:c.-204+8C>T ENSP00000428884.1:n.-204+8C>T
ENST00000613472.1:c.32-9449C>T ENSP00000480778.1:n.32-9449C>T
NM_003844.3:c.403+8C>T NP_003835.3:n.403+8C>T
NM_003844.4:c.403+8C>T MANE Select NP_003835.3:n.403+8C>T