Canonical Allele Identifier: CA370568612
Gene: TNFRSF10A HGNC NCBI

Linked Data

COSMIC: COSM6439657
MyVariant Identifiers: chr8:g.23049317C>T (hg19) chr8:g.23191804C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191804C>T , CM000670.2:g.23191804C>T GRCh38
NC_000008.10:g.23049317C>T , CM000670.1:g.23049317C>T GRCh37
NC_000008.9:g.23105262C>T NCBI36
NG_032107.1:g.38364G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1297G>A MANE Select ENSP00000221132.3:p.Glu433Lys
ENST00000221132.7:c.1297G>A ENSP00000221132.3:p.Glu433Lys
ENST00000613472.1:c.823G>A ENSP00000480778.1:p.Glu275Lys
NM_003844.3:c.1297G>A NP_003835.3:p.Glu433Lys
NM_003844.4:c.1297G>A MANE Select NP_003835.3:p.Glu433Lys
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Search 100 bp 3'