Canonical Allele Identifier: CA1770756054
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212129C= , CM000670.2:g.23212129C= GRCh38
NC_000008.10:g.23069642C= , CM000670.1:g.23069642C= GRCh37
NC_000008.9:g.23125587C= NCBI36
NG_032107.1:g.18039G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.390G= MANE Select ENSP00000221132.3:p.Glu130=
ENST00000221132.7:c.390G= ENSP00000221132.3:p.Glu130=
ENST00000524158.5:c.-217G= ENSP00000428884.1:n.-217G=
ENST00000613472.1:c.32-9470G= ENSP00000480778.1:n.32-9470G=
NM_003844.3:c.390G= NP_003835.3:p.Glu130=
NM_003844.4:c.390G= MANE Select NP_003835.3:p.Glu130=