Canonical Allele Identifier: CA849990197

Gene: TNFRSF10A

Linked Data

• dbSNP Id: rs766974396
• MyVariant Identifiers: chr8:g.23069626T>A (hg19) ; chr8:g.23212113T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212113T>A , CM000670.2:g.23212113T>A	GRCh38
NC_000008.10:g.23069626T>A , CM000670.1:g.23069626T>A	GRCh37
NC_000008.9:g.23125571T>A	NCBI36
NG_032107.1:g.18055A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.403+3A>T MANE Select	ENSP00000221132.3:n.403+3A>T
ENST00000221132.7:c.403+3A>T	ENSP00000221132.3:n.403+3A>T
ENST00000524158.5:c.-204+3A>T	ENSP00000428884.1:n.-204+3A>T
ENST00000613472.1:c.32-9454A>T	ENSP00000480778.1:n.32-9454A>T
NM_003844.3:c.403+3A>T	NP_003835.3:n.403+3A>T
NM_003844.4:c.403+3A>T MANE Select	NP_003835.3:n.403+3A>T