Canonical Allele Identifier: CA370568881
Gene: TNFRSF10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191842C>G , CM000670.2:g.23191842C>G GRCh38
NC_000008.10:g.23049355C>G , CM000670.1:g.23049355C>G GRCh37
NC_000008.9:g.23105300C>G NCBI36
NG_032107.1:g.38326G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1259G>C MANE Select ENSP00000221132.3:p.Gly420Ala
ENST00000221132.7:c.1259G>C ENSP00000221132.3:p.Gly420Ala
ENST00000519862.1:n.314G>C
ENST00000613472.1:c.785G>C ENSP00000480778.1:p.Gly262Ala
NM_003844.3:c.1259G>C NP_003835.3:p.Gly420Ala
NM_003844.4:c.1259G>C MANE Select NP_003835.3:p.Gly420Ala