Canonical Allele Identifier: CA1420539510
Gene: TNFSF10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172506514A= , CM000665.2:g.172506514A= GRCh38
NC_000003.11:g.172224304A= , CM000665.1:g.172224304A= GRCh37
NC_000003.10:g.173706998A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000241261.7:c.824T= MANE Select ENSP00000241261.2:p.Phe275=
ENST00000241261.6:c.824T= ENSP00000241261.2:p.Phe275=
ENST00000420541.6:c.*370T= ENSP00000389931.2:n.*370T=
NM_001190942.1:c.*370T= NP_001177871.1:n.*370T=
NM_003810.3:c.824T= NP_003801.1:p.Phe275=
NR_033994.1:n.904T=
NM_003810.4:c.824T= MANE Select NP_003801.1:p.Phe275=
NM_001190942.2:c.*370T= NP_001177871.1:n.*370T=
NR_033994.2:n.827T=