Canonical Allele Identifier: CA370569115

Gene: TNFRSF10A

Linked Data

• dbSNP Id: rs1446881047
• MyVariant Identifiers: chr8:g.23049381C>T (hg19) ; chr8:g.23191868C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23191868C>T , CM000670.2:g.23191868C>T	GRCh38
NC_000008.10:g.23049381C>T , CM000670.1:g.23049381C>T	GRCh37
NC_000008.9:g.23105326C>T	NCBI36
NG_032107.1:g.38300G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.1233G>A MANE Select	ENSP00000221132.3:p.Met411Ile
ENST00000221132.7:c.1233G>A	ENSP00000221132.3:p.Met411Ile
ENST00000519862.1:n.288G>A
ENST00000613472.1:c.759G>A	ENSP00000480778.1:p.Met253Ile
NM_003844.3:c.1233G>A	NP_003835.3:p.Met411Ile
NM_003844.4:c.1233G>A MANE Select	NP_003835.3:p.Met411Ile