Canonical Allele Identifier: CA355537307
Gene: TNFSF10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172224306A>T (hg19) chr3:g.172506516A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172506516A>T , CM000665.2:g.172506516A>T GRCh38
NC_000003.11:g.172224306A>T , CM000665.1:g.172224306A>T GRCh37
NC_000003.10:g.173707000A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000241261.7:c.822T>A MANE Select ENSP00000241261.2:p.Phe274Leu
ENST00000241261.6:c.822T>A ENSP00000241261.2:p.Phe274Leu
ENST00000420541.6:c.*368T>A ENSP00000389931.2:n.*368T>A
NM_001190942.1:c.*368T>A NP_001177871.1:n.*368T>A
NM_003810.3:c.822T>A NP_003801.1:p.Phe274Leu
NR_033994.1:n.902T>A
NM_003810.4:c.822T>A MANE Select NP_003801.1:p.Phe274Leu
NM_001190942.2:c.*368T>A NP_001177871.1:n.*368T>A
NR_033994.2:n.825T>A
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