Canonical Allele Identifier: CA370583121
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23069638A>C (hg19) chr8:g.23212125A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212125A>C , CM000670.2:g.23212125A>C GRCh38
NC_000008.10:g.23069638A>C , CM000670.1:g.23069638A>C GRCh37
NC_000008.9:g.23125583A>C NCBI36
NG_032107.1:g.18043T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.394T>G MANE Select ENSP00000221132.3:p.Cys132Gly
ENST00000221132.7:c.394T>G ENSP00000221132.3:p.Cys132Gly
ENST00000524158.5:c.-213T>G ENSP00000428884.1:n.-213T>G
ENST00000613472.1:c.32-9466T>G ENSP00000480778.1:n.32-9466T>G
NM_003844.3:c.394T>G NP_003835.3:p.Cys132Gly
NM_003844.4:c.394T>G MANE Select NP_003835.3:p.Cys132Gly
Search 100 bp 5'
Search 100 bp 3'