Canonical Allele Identifier: CA355537329

Gene: TNFSF10

Linked Data

• MyVariant Identifiers: chr3:g.172224316T>A (hg19) ; chr3:g.172506526T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172506526T>A , CM000665.2:g.172506526T>A	GRCh38
NC_000003.11:g.172224316T>A , CM000665.1:g.172224316T>A	GRCh37
NC_000003.10:g.173707010T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000241261.7:c.812A>T MANE Select	ENSP00000241261.2:p.Glu271Val
ENST00000241261.6:c.812A>T	ENSP00000241261.2:p.Glu271Val
ENST00000420541.6:c.*358A>T	ENSP00000389931.2:n.*358A>T
NM_001190942.1:c.*358A>T	NP_001177871.1:n.*358A>T
NM_003810.3:c.812A>T	NP_003801.1:p.Glu271Val
NR_033994.1:n.892A>T
NM_003810.4:c.812A>T MANE Select	NP_003801.1:p.Glu271Val
NM_001190942.2:c.*358A>T	NP_001177871.1:n.*358A>T
NR_033994.2:n.815A>T