Canonical Allele Identifier: CA370568508

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23049308C>A (hg19) ; chr8:g.23191795C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23191795C>A , CM000670.2:g.23191795C>A	GRCh38
NC_000008.10:g.23049308C>A , CM000670.1:g.23049308C>A	GRCh37
NC_000008.9:g.23105253C>A	NCBI36
NG_032107.1:g.38373G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.1306G>T MANE Select	ENSP00000221132.3:p.Glu436Ter
ENST00000221132.7:c.1306G>T	ENSP00000221132.3:p.Glu436Ter
ENST00000613472.1:c.832G>T	ENSP00000480778.1:p.Glu278Ter
NM_003844.3:c.1306G>T	NP_003835.3:p.Glu436Ter
NM_003844.4:c.1306G>T MANE Select	NP_003835.3:p.Glu436Ter