Canonical Allele Identifier: CA370576614
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23058228A>T (hg19) chr8:g.23200715A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23200715A>T , CM000670.2:g.23200715A>T GRCh38
NC_000008.10:g.23058228A>T , CM000670.1:g.23058228A>T GRCh37
NC_000008.9:g.23114173A>T NCBI36
NG_032107.1:g.29453T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.675T>A MANE Select ENSP00000221132.3:p.Ser225Arg
ENST00000221132.7:c.675T>A ENSP00000221132.3:p.Ser225Arg
ENST00000524158.5:c.69T>A ENSP00000428884.1:p.Ser23Arg
ENST00000613472.1:c.201T>A ENSP00000480778.1:p.Ser67Arg
NM_003844.3:c.675T>A NP_003835.3:p.Ser225Arg
NM_003844.4:c.675T>A MANE Select NP_003835.3:p.Ser225Arg
Search 100 bp 5'
Search 100 bp 3'