Canonical Allele Identifier: CA4674550
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs2230229
gnomAD v2: 8-23049292-C-T
gnomAD v3: 8-23191779-C-T
gnomAD v4: 8-23191779-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191779C>T , CM000670.2:g.23191779C>T GRCh38
NC_000008.10:g.23049292C>T , CM000670.1:g.23049292C>T GRCh37
NC_000008.9:g.23105237C>T NCBI36
NG_032107.1:g.38389G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1322G>A MANE Select ENSP00000221132.3:p.Arg441Lys
ENST00000221132.7:c.1322G>A ENSP00000221132.3:p.Arg441Lys
ENST00000613472.1:c.848G>A ENSP00000480778.1:p.Arg283Lys
NM_003844.3:c.1322G>A NP_003835.3:p.Arg441Lys
NM_003844.4:c.1322G>A MANE Select NP_003835.3:p.Arg441Lys