Canonical Allele Identifier: CA2014026066

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333436A= , CM000674.2:g.6333436A=	GRCh38
NC_000012.11:g.6442602A= , CM000674.1:g.6442602A=	GRCh37
NC_000012.10:g.6312863A=	NCBI36
NG_007506.1:g.13660T= , LRG_193:g.13660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.437T=
ENST00000437813.8:c.403T=	ENSP00000513672.1:p.Tyr135=
ENST00000440083.7:c.403T=	ENSP00000413224.3:p.Tyr135=
ENST00000535958.2:c.*230T=	ENSP00000513673.1:n.*230T=
ENST00000698339.1:c.403T=	ENSP00000513670.1:p.Tyr135=
ENST00000698340.1:c.403T=	ENSP00000513671.1:p.Tyr135=
ENST00000162749.7:c.403T= MANE Select	ENSP00000162749.2:p.Tyr135=
ENST00000162749.6:c.403T=	ENSP00000162749.2:p.Tyr135=
ENST00000366159.8:c.403T=	ENSP00000380389.3:p.Tyr135=
ENST00000437813.7:n.364T=
ENST00000440083.6:c.403T=	ENSP00000413224.2:p.Tyr135=
ENST00000534885.5:c.249T=	ENSP00000441803.1:p.Ile83=
ENST00000537842.5:n.7T=
ENST00000539372.5:c.403T=	ENSP00000442059.1:p.Tyr135=
ENST00000540022.5:c.274T=	ENSP00000438343.1:p.Tyr92=
ENST00000543048.5:c.*14T=	ENSP00000439981.1:n.*14T=
ENST00000543995.5:c.209T=	ENSP00000442405.1:p.Leu70=
NM_001065.3:c.403T= , LRG_193t1:c.403T=	NP_001056.1:p.Tyr135=
NM_001346091.1:c.79T=	NP_001333020.1:p.Tyr27=
NM_001346092.1:c.-175T=	NP_001333021.1:n.-175T=
NR_144351.1:n.706T=
NM_001065.4:c.403T= MANE Select	NP_001056.1:p.Tyr135=
NM_001346091.2:c.79T=	NP_001333020.1:p.Tyr27=
NM_001346092.2:c.-175T=	NP_001333021.1:n.-175T=
NR_144351.2:n.665T=