Canonical Allele Identifier: CA459967600

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23069645T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212132T>G , CM000670.2:g.23212132T>G	GRCh38
NC_000008.10:g.23069645T>G , CM000670.1:g.23069645T>G	GRCh37
NC_000008.9:g.23125590T>G	NCBI36
NG_032107.1:g.18036A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.387A>C MANE Select	ENSP00000221132.3:p.Gly129=
ENST00000221132.7:c.387A>C	ENSP00000221132.3:p.Gly129=
ENST00000524158.5:c.-220A>C	ENSP00000428884.1:n.-220A>C
ENST00000613472.1:c.32-9473A>C	ENSP00000480778.1:n.32-9473A>C
NM_003844.3:c.387A>C	NP_003835.3:p.Gly129=
NM_003844.4:c.387A>C MANE Select	NP_003835.3:p.Gly129=