Canonical Allele Identifier: CA459967888

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23069717A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212204A>T , CM000670.2:g.23212204A>T	GRCh38
NC_000008.10:g.23069717A>T , CM000670.1:g.23069717A>T	GRCh37
NC_000008.9:g.23125662A>T	NCBI36
NG_032107.1:g.17964T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.315T>A MANE Select	ENSP00000221132.3:p.Pro105=
ENST00000221132.7:c.315T>A	ENSP00000221132.3:p.Pro105=
ENST00000524158.5:c.-292T>A	ENSP00000428884.1:n.-292T>A
ENST00000613472.1:c.32-9545T>A	ENSP00000480778.1:n.32-9545T>A
NM_003844.3:c.315T>A	NP_003835.3:p.Pro105=
NM_003844.4:c.315T>A MANE Select	NP_003835.3:p.Pro105=