Canonical Allele Identifier: CA1770771580
Gene: TNFRSF10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23200714C= , CM000670.2:g.23200714C= GRCh38
NC_000008.10:g.23058227C= , CM000670.1:g.23058227C= GRCh37
NC_000008.9:g.23114172C= NCBI36
NG_032107.1:g.29454G=

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.676G= MANE Select ENSP00000221132.3:p.Asp226=
ENST00000221132.7:c.676G= ENSP00000221132.3:p.Asp226=
ENST00000524158.5:c.70G= ENSP00000428884.1:p.Asp24=
ENST00000613472.1:c.202G= ENSP00000480778.1:p.Asp68=
NM_003844.3:c.676G= NP_003835.3:p.Asp226=
NM_003844.4:c.676G= MANE Select NP_003835.3:p.Asp226=