Canonical Allele Identifier: CA370583226

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23069674T>A (hg19) ; chr8:g.23212161T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212161T>A , CM000670.2:g.23212161T>A	GRCh38
NC_000008.10:g.23069674T>A , CM000670.1:g.23069674T>A	GRCh37
NC_000008.9:g.23125619T>A	NCBI36
NG_032107.1:g.18007A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.358A>T MANE Select	ENSP00000221132.3:p.Thr120Ser
ENST00000221132.7:c.358A>T	ENSP00000221132.3:p.Thr120Ser
ENST00000524158.5:c.-249A>T	ENSP00000428884.1:n.-249A>T
ENST00000613472.1:c.32-9502A>T	ENSP00000480778.1:n.32-9502A>T
NM_003844.3:c.358A>T	NP_003835.3:p.Thr120Ser
NM_003844.4:c.358A>T MANE Select	NP_003835.3:p.Thr120Ser