Canonical Allele Identifier: CA370568636

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23049320A>C (hg19) ; chr8:g.23191807A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23191807A>C , CM000670.2:g.23191807A>C	GRCh38
NC_000008.10:g.23049320A>C , CM000670.1:g.23049320A>C	GRCh37
NC_000008.9:g.23105265A>C	NCBI36
NG_032107.1:g.38361T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.1294T>G MANE Select	ENSP00000221132.3:p.Leu432Val
ENST00000221132.7:c.1294T>G	ENSP00000221132.3:p.Leu432Val
ENST00000613472.1:c.820T>G	ENSP00000480778.1:p.Leu274Val
NM_003844.3:c.1294T>G	NP_003835.3:p.Leu432Val
NM_003844.4:c.1294T>G MANE Select	NP_003835.3:p.Leu432Val