Canonical Allele Identifier: CA2014024245

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330892G= , CM000674.2:g.6330892G=	GRCh38
NC_000012.11:g.6440058G= , CM000674.1:g.6440058G=	GRCh37
NC_000012.10:g.6310319G=	NCBI36
NG_007506.1:g.16204C= , LRG_193:g.16204C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1687C=
ENST00000437813.8:c.*47C=	ENSP00000513672.1:n.*47C=
ENST00000440083.7:c.805C=	ENSP00000413224.3:p.Leu269=
ENST00000535038.2:n.768C=
ENST00000535958.2:c.*413C=	ENSP00000513673.1:n.*413C=
ENST00000698337.1:n.435C=
ENST00000698338.1:n.859C=
ENST00000698339.1:c.*81C=	ENSP00000513670.1:n.*81C=
ENST00000698340.1:c.552-181C=	ENSP00000513671.1:n.552-181C=
ENST00000162749.7:c.586C= MANE Select	ENSP00000162749.2:p.Leu196=
ENST00000162749.6:c.586C=	ENSP00000162749.2:p.Leu196=
ENST00000534885.5:c.*63C=	ENSP00000441803.1:n.*63C=
ENST00000535038.1:n.256C=
ENST00000536717.5:n.490C=
ENST00000537842.5:n.190C=
ENST00000539372.5:c.586C=	ENSP00000442059.1:p.Leu196=
ENST00000540022.5:c.457C=	ENSP00000438343.1:p.Leu153=
ENST00000543359.5:n.38-181C=
ENST00000543995.5:c.*173C=	ENSP00000442405.1:n.*173C=
NM_001065.3:c.586C= , LRG_193t1:c.586C=	NP_001056.1:p.Leu196=
NM_001346091.1:c.262C=	NP_001333020.1:p.Leu88=
NM_001346092.1:c.127C=	NP_001333021.1:p.Leu43=
NR_144351.1:n.855-181C=
NM_001065.4:c.586C= MANE Select	NP_001056.1:p.Leu196=
NM_001346091.2:c.262C=	NP_001333020.1:p.Leu88=
NM_001346092.2:c.127C=	NP_001333021.1:p.Leu43=
NR_144351.2:n.814-181C=