Canonical Allele Identifier: CA1770756291

Gene: TNFRSF10A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212190G= , CM000670.2:g.23212190G=	GRCh38
NC_000008.10:g.23069703G= , CM000670.1:g.23069703G=	GRCh37
NC_000008.9:g.23125648G=	NCBI36
NG_032107.1:g.17978C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.329C= MANE Select	ENSP00000221132.3:p.Thr110=
ENST00000221132.7:c.329C=	ENSP00000221132.3:p.Thr110=
ENST00000524158.5:c.-278C=	ENSP00000428884.1:n.-278C=
ENST00000613472.1:c.32-9531C=	ENSP00000480778.1:n.32-9531C=
NM_003844.3:c.329C=	NP_003835.3:p.Thr110=
NM_003844.4:c.329C= MANE Select	NP_003835.3:p.Thr110=