Canonical Allele Identifier: CA370583184
Gene: TNFRSF10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212151C>G , CM000670.2:g.23212151C>G GRCh38
NC_000008.10:g.23069664C>G , CM000670.1:g.23069664C>G GRCh37
NC_000008.9:g.23125609C>G NCBI36
NG_032107.1:g.18017G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.368G>C MANE Select ENSP00000221132.3:p.Trp123Ser
ENST00000221132.7:c.368G>C ENSP00000221132.3:p.Trp123Ser
ENST00000524158.5:c.-239G>C ENSP00000428884.1:n.-239G>C
ENST00000613472.1:c.32-9492G>C ENSP00000480778.1:n.32-9492G>C
NM_003844.3:c.368G>C NP_003835.3:p.Trp123Ser
NM_003844.4:c.368G>C MANE Select NP_003835.3:p.Trp123Ser