Canonical Allele Identifier: CA1770756180
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212164C= , CM000670.2:g.23212164C= GRCh38
NC_000008.10:g.23069677C= , CM000670.1:g.23069677C= GRCh37
NC_000008.9:g.23125622C= NCBI36
NG_032107.1:g.18004G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.355G= MANE Select ENSP00000221132.3:p.Gly119=
ENST00000221132.7:c.355G= ENSP00000221132.3:p.Gly119=
ENST00000524158.5:c.-252G= ENSP00000428884.1:n.-252G=
ENST00000613472.1:c.32-9505G= ENSP00000480778.1:n.32-9505G=
NM_003844.3:c.355G= NP_003835.3:p.Gly119=
NM_003844.4:c.355G= MANE Select NP_003835.3:p.Gly119=