Canonical Allele Identifier: CA2014024265

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330915C= , CM000674.2:g.6330915C=	GRCh38
NC_000012.11:g.6440081C= , CM000674.1:g.6440081C=	GRCh37
NC_000012.10:g.6310342C=	NCBI36
NG_007506.1:g.16181G= , LRG_193:g.16181G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1664G=
ENST00000437813.8:c.*24G=	ENSP00000513672.1:n.*24G=
ENST00000440083.7:c.782G=	ENSP00000413224.3:p.Ser261=
ENST00000535038.2:n.745G=
ENST00000535958.2:c.*390G=	ENSP00000513673.1:n.*390G=
ENST00000698337.1:n.412G=
ENST00000698338.1:n.836G=
ENST00000698339.1:c.*58G=	ENSP00000513670.1:n.*58G=
ENST00000698340.1:c.552-204G=	ENSP00000513671.1:n.552-204G=
ENST00000162749.7:c.563G= MANE Select	ENSP00000162749.2:p.Ser188=
ENST00000162749.6:c.563G=	ENSP00000162749.2:p.Ser188=
ENST00000534885.5:c.*40G=	ENSP00000441803.1:n.*40G=
ENST00000535038.1:n.233G=
ENST00000536717.5:n.467G=
ENST00000537842.5:n.167G=
ENST00000539372.5:c.563G=	ENSP00000442059.1:p.Ser188=
ENST00000540022.5:c.434G=	ENSP00000438343.1:p.Ser145=
ENST00000543359.5:n.38-204G=
ENST00000543995.5:c.*150G=	ENSP00000442405.1:n.*150G=
NM_001065.3:c.563G= , LRG_193t1:c.563G=	NP_001056.1:p.Ser188=
NM_001346091.1:c.239G=	NP_001333020.1:p.Ser80=
NM_001346092.1:c.104G=	NP_001333021.1:p.Ser35=
NR_144351.1:n.855-204G=
NM_001065.4:c.563G= MANE Select	NP_001056.1:p.Ser188=
NM_001346091.2:c.239G=	NP_001333020.1:p.Ser80=
NM_001346092.2:c.104G=	NP_001333021.1:p.Ser35=
NR_144351.2:n.814-204G=