Canonical Allele Identifier: CA1770756397
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212211A= , CM000670.2:g.23212211A= GRCh38
NC_000008.10:g.23069724A= , CM000670.1:g.23069724A= GRCh37
NC_000008.9:g.23125669A= NCBI36
NG_032107.1:g.17957T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.308T= MANE Select ENSP00000221132.3:p.Val103=
ENST00000221132.7:c.308T= ENSP00000221132.3:p.Val103=
ENST00000524158.5:c.-299T= ENSP00000428884.1:n.-299T=
ENST00000613472.1:c.32-9552T= ENSP00000480778.1:n.32-9552T=
NM_003844.3:c.308T= NP_003835.3:p.Val103=
NM_003844.4:c.308T= MANE Select NP_003835.3:p.Val103=