Canonical Allele Identifier: CA4674945

Gene: TNFRSF10A

Linked Data

• ClinVar Variation Id: 2539088
• ClinVar RCV Id: RCV004311446
• dbSNP Id: rs200630980
• ExAC: 8:23069635 G / A
• gnomAD v2: 8-23069635-G-A
• gnomAD v3: 8-23212122-G-A
• gnomAD v4: 8-23212122-G-A
• MyVariant Identifiers: chr8:g.23069635G>A (hg19) ; chr8:g.23212122G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212122G>A , CM000670.2:g.23212122G>A	GRCh38
NC_000008.10:g.23069635G>A , CM000670.1:g.23069635G>A	GRCh37
NC_000008.9:g.23125580G>A	NCBI36
NG_032107.1:g.18046C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.397C>T MANE Select	ENSP00000221132.3:p.Pro133Ser
ENST00000221132.7:c.397C>T	ENSP00000221132.3:p.Pro133Ser
ENST00000524158.5:c.-210C>T	ENSP00000428884.1:n.-210C>T
ENST00000613472.1:c.32-9463C>T	ENSP00000480778.1:n.32-9463C>T
NM_003844.3:c.397C>T	NP_003835.3:p.Pro133Ser
NM_003844.4:c.397C>T MANE Select	NP_003835.3:p.Pro133Ser