Canonical Allele Identifier: CA580952719
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1304811811
gnomAD v2: 8-23049346-G-GTCGC
gnomAD v3: 8-23191833-G-GTCGC
gnomAD v4: 8-23191833-G-GTCGC
MyVariant Identifiers: chr8:g.23049346_23049347insTCGC (hg19) chr8:g.23191833_23191834insTCGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191833_23191834insTCGC , CM000670.2:g.23191833_23191834insTCGC GRCh38
NC_000008.10:g.23049346_23049347insTCGC , CM000670.1:g.23049346_23049347insTCGC GRCh37
NC_000008.9:g.23105291_23105292insTCGC NCBI36
NG_032107.1:g.38334_38335insGCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1267_1268insGCGA MANE Select ENSP00000221132.3:p.Ala423GlyfsTer?
ENST00000221132.7:c.1267_1268insGCGA ENSP00000221132.3:p.Ala423GlyfsTer?
ENST00000519862.1:n.322_323insGCGA
ENST00000613472.1:c.793_794insGCGA ENSP00000480778.1:p.Ala265GlyfsTer?
NM_003844.3:c.1267_1268insGCGA NP_003835.3:p.Ala423GlyfsTer?
NM_003844.4:c.1267_1268insGCGA MANE Select NP_003835.3:p.Ala423GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'