Canonical Allele Identifier: CA460179435

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23049354T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23191841T>A , CM000670.2:g.23191841T>A	GRCh38
NC_000008.10:g.23049354T>A , CM000670.1:g.23049354T>A	GRCh37
NC_000008.9:g.23105299T>A	NCBI36
NG_032107.1:g.38327A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.1260A>T MANE Select	ENSP00000221132.3:p.Gly420=
ENST00000221132.7:c.1260A>T	ENSP00000221132.3:p.Gly420=
ENST00000519862.1:n.315A>T
ENST00000613472.1:c.786A>T	ENSP00000480778.1:p.Gly262=
NM_003844.3:c.1260A>T	NP_003835.3:p.Gly420=
NM_003844.4:c.1260A>T MANE Select	NP_003835.3:p.Gly420=