Canonical Allele Identifier: CA370583125

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23069639C>G (hg19) ; chr8:g.23212126C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212126C>G , CM000670.2:g.23212126C>G	GRCh38
NC_000008.10:g.23069639C>G , CM000670.1:g.23069639C>G	GRCh37
NC_000008.9:g.23125584C>G	NCBI36
NG_032107.1:g.18042G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.393G>C MANE Select	ENSP00000221132.3:p.Leu131Phe
ENST00000221132.7:c.393G>C	ENSP00000221132.3:p.Leu131Phe
ENST00000524158.5:c.-214G>C	ENSP00000428884.1:n.-214G>C
ENST00000613472.1:c.32-9467G>C	ENSP00000480778.1:n.32-9467G>C
NM_003844.3:c.393G>C	NP_003835.3:p.Leu131Phe
NM_003844.4:c.393G>C MANE Select	NP_003835.3:p.Leu131Phe