Canonical Allele Identifier: CA1770754361
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191859T= , CM000670.2:g.23191859T= GRCh38
NC_000008.10:g.23049372T= , CM000670.1:g.23049372T= GRCh37
NC_000008.9:g.23105317T= NCBI36
NG_032107.1:g.38309A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1242A= MANE Select ENSP00000221132.3:p.Lys414=
ENST00000221132.7:c.1242A= ENSP00000221132.3:p.Lys414=
ENST00000519862.1:n.297A=
ENST00000613472.1:c.768A= ENSP00000480778.1:p.Lys256=
NM_003844.3:c.1242A= NP_003835.3:p.Lys414=
NM_003844.4:c.1242A= MANE Select NP_003835.3:p.Lys414=