Canonical Allele Identifier: CA1770756119

Gene: TNFRSF10A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212148T= , CM000670.2:g.23212148T=	GRCh38
NC_000008.10:g.23069661T= , CM000670.1:g.23069661T=	GRCh37
NC_000008.9:g.23125606T=	NCBI36
NG_032107.1:g.18020A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.371A= MANE Select	ENSP00000221132.3:p.Glu124=
ENST00000221132.7:c.371A=	ENSP00000221132.3:p.Glu124=
ENST00000524158.5:c.-236A=	ENSP00000428884.1:n.-236A=
ENST00000613472.1:c.32-9489A=	ENSP00000480778.1:n.32-9489A=
NM_003844.3:c.371A=	NP_003835.3:p.Glu124=
NM_003844.4:c.371A= MANE Select	NP_003835.3:p.Glu124=