Canonical Allele Identifier: CA1770755928
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212089G= , CM000670.2:g.23212089G= GRCh38
NC_000008.10:g.23069602G= , CM000670.1:g.23069602G= GRCh37
NC_000008.9:g.23125547G= NCBI36
NG_032107.1:g.18079C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.403+27C= MANE Select ENSP00000221132.3:n.403+27C=
ENST00000221132.7:c.403+27C= ENSP00000221132.3:n.403+27C=
ENST00000524158.5:c.-204+27C= ENSP00000428884.1:n.-204+27C=
ENST00000613472.1:c.32-9430C= ENSP00000480778.1:n.32-9430C=
NM_003844.3:c.403+27C= NP_003835.3:n.403+27C=
NM_003844.4:c.403+27C= MANE Select NP_003835.3:n.403+27C=