Canonical Allele Identifier: CA2014025888

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333126A= , CM000674.2:g.6333126A=	GRCh38
NC_000012.11:g.6442292A= , CM000674.1:g.6442292A=	GRCh37
NC_000012.10:g.6312553A=	NCBI36
NG_007506.1:g.13970T= , LRG_193:g.13970T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.528T=
ENST00000437813.8:c.494T=	ENSP00000513672.1:p.Val165=
ENST00000440083.7:c.713T=	ENSP00000413224.3:p.Val238=
ENST00000535958.2:c.*321T=	ENSP00000513673.1:n.*321T=
ENST00000698339.1:c.494T=	ENSP00000513670.1:p.Val165=
ENST00000698340.1:c.494T=	ENSP00000513671.1:p.Val165=
ENST00000162749.7:c.494T= MANE Select	ENSP00000162749.2:p.Val165=
ENST00000162749.6:c.494T=	ENSP00000162749.2:p.Val165=
ENST00000366159.8:c.494T=	ENSP00000380389.3:p.Val165=
ENST00000437813.7:n.455T=
ENST00000440083.6:c.713T=	ENSP00000413224.2:p.Val238=
ENST00000534885.5:c.340T=	ENSP00000441803.1:p.Cys114=
ENST00000537842.5:n.98T=
ENST00000539372.5:c.494T=	ENSP00000442059.1:p.Val165=
ENST00000540022.5:c.365T=	ENSP00000438343.1:p.Val122=
ENST00000543048.5:c.*105T=	ENSP00000439981.1:n.*105T=
ENST00000543995.5:c.*81T=	ENSP00000442405.1:n.*81T=
NM_001065.3:c.494T= , LRG_193t1:c.494T=	NP_001056.1:p.Val165=
NM_001346091.1:c.170T=	NP_001333020.1:p.Val57=
NM_001346092.1:c.-84T=	NP_001333021.1:n.-84T=
NR_144351.1:n.797T=
NM_001065.4:c.494T= MANE Select	NP_001056.1:p.Val165=
NM_001346091.2:c.170T=	NP_001333020.1:p.Val57=
NM_001346092.2:c.-84T=	NP_001333021.1:n.-84T=
NR_144351.2:n.756T=