Canonical Allele Identifier: CA2014026232

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333776G= , CM000674.2:g.6333776G=	GRCh38
NC_000012.11:g.6442942G= , CM000674.1:g.6442942G=	GRCh37
NC_000012.10:g.6313203G=	NCBI36
NG_007506.1:g.13320C= , LRG_193:g.13320C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.317C=
ENST00000437813.8:c.283C=	ENSP00000513672.1:p.His95=
ENST00000440083.7:c.283C=	ENSP00000413224.3:p.His95=
ENST00000535958.2:c.*110C=	ENSP00000513673.1:n.*110C=
ENST00000698339.1:c.283C=	ENSP00000513670.1:p.His95=
ENST00000698340.1:c.283C=	ENSP00000513671.1:p.His95=
ENST00000162749.7:c.283C= MANE Select	ENSP00000162749.2:p.His95=
ENST00000162749.6:c.283C=	ENSP00000162749.2:p.His95=
ENST00000366159.8:c.283C=	ENSP00000380389.3:p.His95=
ENST00000437813.7:n.244C=
ENST00000440083.6:c.283C=	ENSP00000413224.2:p.His95=
ENST00000534885.5:c.129C=	ENSP00000441803.1:p.Thr43=
ENST00000535958.1:n.529C=
ENST00000536194.1:c.256C=	ENSP00000442919.1:p.His86=
ENST00000539372.5:c.283C=	ENSP00000442059.1:p.His95=
ENST00000540022.5:c.194-260C=	ENSP00000438343.1:n.194-260C=
ENST00000543048.5:c.214+69C=	ENSP00000439981.1:n.214+69C=
ENST00000543995.5:c.193+315C=	ENSP00000442405.1:n.193+315C=
NM_001065.3:c.283C= , LRG_193t1:c.283C=	NP_001056.1:p.His95=
NM_001346091.1:c.-42C=	NP_001333020.1:n.-42C=
NM_001346092.1:c.-295C=	NP_001333021.1:n.-295C=
NR_144351.1:n.586C=
NM_001065.4:c.283C= MANE Select	NP_001056.1:p.His95=
NM_001346091.2:c.-42C=	NP_001333020.1:n.-42C=
NM_001346092.2:c.-295C=	NP_001333021.1:n.-295C=
NR_144351.2:n.545C=