Canonical Allele Identifier: CA370576590
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23058224T>G (hg19) chr8:g.23200711T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23200711T>G , CM000670.2:g.23200711T>G GRCh38
NC_000008.10:g.23058224T>G , CM000670.1:g.23058224T>G GRCh37
NC_000008.9:g.23114169T>G NCBI36
NG_032107.1:g.29457A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.679A>C MANE Select ENSP00000221132.3:p.Ile227Leu
ENST00000221132.7:c.679A>C ENSP00000221132.3:p.Ile227Leu
ENST00000524158.5:c.73A>C ENSP00000428884.1:p.Ile25Leu
ENST00000613472.1:c.205A>C ENSP00000480778.1:p.Ile69Leu
NM_003844.3:c.679A>C NP_003835.3:p.Ile227Leu
NM_003844.4:c.679A>C MANE Select NP_003835.3:p.Ile227Leu
Search 100 bp 5'
Search 100 bp 3'