Canonical Allele Identifier: CA4674572
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs767538728
gnomAD v2: 8-23049383-T-C
gnomAD v4: 8-23191870-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191870T>C , CM000670.2:g.23191870T>C GRCh38
NC_000008.10:g.23049383T>C , CM000670.1:g.23049383T>C GRCh37
NC_000008.9:g.23105328T>C NCBI36
NG_032107.1:g.38298A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1231A>G MANE Select ENSP00000221132.3:p.Met411Val
ENST00000221132.7:c.1231A>G ENSP00000221132.3:p.Met411Val
ENST00000519862.1:n.286A>G
ENST00000613472.1:c.757A>G ENSP00000480778.1:p.Met253Val
NM_003844.3:c.1231A>G NP_003835.3:p.Met411Val
NM_003844.4:c.1231A>G MANE Select NP_003835.3:p.Met411Val