Canonical Allele Identifier: CA370583123

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23069638A>T (hg19) ; chr8:g.23212125A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212125A>T , CM000670.2:g.23212125A>T	GRCh38
NC_000008.10:g.23069638A>T , CM000670.1:g.23069638A>T	GRCh37
NC_000008.9:g.23125583A>T	NCBI36
NG_032107.1:g.18043T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.394T>A MANE Select	ENSP00000221132.3:p.Cys132Ser
ENST00000221132.7:c.394T>A	ENSP00000221132.3:p.Cys132Ser
ENST00000524158.5:c.-213T>A	ENSP00000428884.1:n.-213T>A
ENST00000613472.1:c.32-9466T>A	ENSP00000480778.1:n.32-9466T>A
NM_003844.3:c.394T>A	NP_003835.3:p.Cys132Ser
NM_003844.4:c.394T>A MANE Select	NP_003835.3:p.Cys132Ser