Canonical Allele Identifier: CA2014026091

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333490A= , CM000674.2:g.6333490A=	GRCh38
NC_000012.11:g.6442656A= , CM000674.1:g.6442656A=	GRCh37
NC_000012.10:g.6312917A=	NCBI36
NG_007506.1:g.13606T= , LRG_193:g.13606T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.383T=
ENST00000437813.8:c.349T=	ENSP00000513672.1:p.Cys117=
ENST00000440083.7:c.349T=	ENSP00000413224.3:p.Cys117=
ENST00000535958.2:c.*176T=	ENSP00000513673.1:n.*176T=
ENST00000698339.1:c.349T=	ENSP00000513670.1:p.Cys117=
ENST00000698340.1:c.349T=	ENSP00000513671.1:p.Cys117=
ENST00000162749.7:c.349T= MANE Select	ENSP00000162749.2:p.Cys117=
ENST00000162749.6:c.349T=	ENSP00000162749.2:p.Cys117=
ENST00000366159.8:c.349T=	ENSP00000380389.3:p.Cys117=
ENST00000437813.7:n.310T=
ENST00000440083.6:c.349T=	ENSP00000413224.2:p.Cys117=
ENST00000534885.5:c.195T=	ENSP00000441803.1:p.Leu65=
ENST00000536194.1:c.322T=	ENSP00000442919.1:p.Cys108=
ENST00000539372.5:c.349T=	ENSP00000442059.1:p.Cys117=
ENST00000540022.5:c.220T=	ENSP00000438343.1:p.Cys74=
ENST00000543048.5:c.215-39T=	ENSP00000439981.1:n.215-39T=
ENST00000543995.5:c.194-39T=	ENSP00000442405.1:n.194-39T=
NM_001065.3:c.349T= , LRG_193t1:c.349T=	NP_001056.1:p.Cys117=
NM_001346091.1:c.25T=	NP_001333020.1:p.Cys9=
NM_001346092.1:c.-229T=	NP_001333021.1:n.-229T=
NR_144351.1:n.652T=
NM_001065.4:c.349T= MANE Select	NP_001056.1:p.Cys117=
NM_001346091.2:c.25T=	NP_001333020.1:p.Cys9=
NM_001346092.2:c.-229T=	NP_001333021.1:n.-229T=
NR_144351.2:n.611T=