Canonical Allele Identifier: CA2014026248

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333805T= , CM000674.2:g.6333805T=	GRCh38
NC_000012.11:g.6442971T= , CM000674.1:g.6442971T=	GRCh37
NC_000012.10:g.6313232T=	NCBI36
NG_007506.1:g.13291A= , LRG_193:g.13291A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.288A=
ENST00000437813.8:c.254A=	ENSP00000513672.1:p.Glu85=
ENST00000440083.7:c.254A=	ENSP00000413224.3:p.Glu85=
ENST00000535958.2:c.*81A=	ENSP00000513673.1:n.*81A=
ENST00000698339.1:c.254A=	ENSP00000513670.1:p.Glu85=
ENST00000698340.1:c.254A=	ENSP00000513671.1:p.Glu85=
ENST00000162749.7:c.254A= MANE Select	ENSP00000162749.2:p.Glu85=
ENST00000162749.6:c.254A=	ENSP00000162749.2:p.Glu85=
ENST00000366159.8:c.254A=	ENSP00000380389.3:p.Glu85=
ENST00000437813.7:n.215A=
ENST00000440083.6:c.254A=	ENSP00000413224.2:p.Glu85=
ENST00000534885.5:c.100A=	ENSP00000441803.1:p.Arg34=
ENST00000535958.1:n.500A=
ENST00000536194.1:c.227A=	ENSP00000442919.1:p.Glu76=
ENST00000539372.5:c.254A=	ENSP00000442059.1:p.Glu85=
ENST00000540022.5:c.193+286A=	ENSP00000438343.1:n.193+286A=
ENST00000543048.5:c.214+40A=	ENSP00000439981.1:n.214+40A=
ENST00000543995.5:c.193+286A=	ENSP00000442405.1:n.193+286A=
NM_001065.3:c.254A= , LRG_193t1:c.254A=	NP_001056.1:p.Glu85=
NM_001346091.1:c.-71A=	NP_001333020.1:n.-71A=
NM_001346092.1:c.-324A=	NP_001333021.1:n.-324A=
NR_144351.1:n.557A=
NM_001065.4:c.254A= MANE Select	NP_001056.1:p.Glu85=
NM_001346091.2:c.-71A=	NP_001333020.1:n.-71A=
NM_001346092.2:c.-324A=	NP_001333021.1:n.-324A=
NR_144351.2:n.516A=