Canonical Allele Identifier: CA2014026247

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333804C= , CM000674.2:g.6333804C=	GRCh38
NC_000012.11:g.6442970C= , CM000674.1:g.6442970C=	GRCh37
NC_000012.10:g.6313231C=	NCBI36
NG_007506.1:g.13292G= , LRG_193:g.13292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.289G=
ENST00000437813.8:c.255G=	ENSP00000513672.1:p.Glu85=
ENST00000440083.7:c.255G=	ENSP00000413224.3:p.Glu85=
ENST00000535958.2:c.*82G=	ENSP00000513673.1:n.*82G=
ENST00000698339.1:c.255G=	ENSP00000513670.1:p.Glu85=
ENST00000698340.1:c.255G=	ENSP00000513671.1:p.Glu85=
ENST00000162749.7:c.255G= MANE Select	ENSP00000162749.2:p.Glu85=
ENST00000162749.6:c.255G=	ENSP00000162749.2:p.Glu85=
ENST00000366159.8:c.255G=	ENSP00000380389.3:p.Glu85=
ENST00000437813.7:n.216G=
ENST00000440083.6:c.255G=	ENSP00000413224.2:p.Glu85=
ENST00000534885.5:c.101G=	ENSP00000441803.1:p.Arg34=
ENST00000535958.1:n.501G=
ENST00000536194.1:c.228G=	ENSP00000442919.1:p.Glu76=
ENST00000539372.5:c.255G=	ENSP00000442059.1:p.Glu85=
ENST00000540022.5:c.194-288G=	ENSP00000438343.1:n.194-288G=
ENST00000543048.5:c.214+41G=	ENSP00000439981.1:n.214+41G=
ENST00000543995.5:c.193+287G=	ENSP00000442405.1:n.193+287G=
NM_001065.3:c.255G= , LRG_193t1:c.255G=	NP_001056.1:p.Glu85=
NM_001346091.1:c.-70G=	NP_001333020.1:n.-70G=
NM_001346092.1:c.-323G=	NP_001333021.1:n.-323G=
NR_144351.1:n.558G=
NM_001065.4:c.255G= MANE Select	NP_001056.1:p.Glu85=
NM_001346091.2:c.-70G=	NP_001333020.1:n.-70G=
NM_001346092.2:c.-323G=	NP_001333021.1:n.-323G=
NR_144351.2:n.517G=