Canonical Allele Identifier: CA370576618

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23058229C>A (hg19) ; chr8:g.23200716C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23200716C>A , CM000670.2:g.23200716C>A	GRCh38
NC_000008.10:g.23058229C>A , CM000670.1:g.23058229C>A	GRCh37
NC_000008.9:g.23114174C>A	NCBI36
NG_032107.1:g.29452G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000221132.8:c.674G>T MANE Select	ENSP00000221132.3:p.Ser225Ile
ENST00000221132.7:c.674G>T	ENSP00000221132.3:p.Ser225Ile
ENST00000524158.5:c.68G>T	ENSP00000428884.1:p.Ser23Ile
ENST00000613472.1:c.200G>T	ENSP00000480778.1:p.Ser67Ile
NM_003844.3:c.674G>T	NP_003835.3:p.Ser225Ile
NM_003844.4:c.674G>T MANE Select	NP_003835.3:p.Ser225Ile