Canonical Allele Identifier: CA1770754335
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191850G= , CM000670.2:g.23191850G= GRCh38
NC_000008.10:g.23049363G= , CM000670.1:g.23049363G= GRCh37
NC_000008.9:g.23105308G= NCBI36
NG_032107.1:g.38318C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1251C= MANE Select ENSP00000221132.3:p.Asn417=
ENST00000221132.7:c.1251C= ENSP00000221132.3:p.Asn417=
ENST00000519862.1:n.306C=
ENST00000613472.1:c.777C= ENSP00000480778.1:p.Asn259=
NM_003844.3:c.1251C= NP_003835.3:p.Asn417=
NM_003844.4:c.1251C= MANE Select NP_003835.3:p.Asn417=