Canonical Allele Identifier: CA2014022931

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329900C= , CM000674.2:g.6329900C=	GRCh38
NC_000012.11:g.6439066C= , CM000674.1:g.6439066C=	GRCh37
NC_000012.10:g.6309327C=	NCBI36
NG_007506.1:g.17196G= , LRG_193:g.17196G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.935G= MANE Select	NP_001056.1:p.Arg312=
ENST00000162749.7:c.935G= MANE Select	ENSP00000162749.2:p.Arg312=
NM_001065.3:c.935G= , LRG_193t1:c.935G=	NP_001056.1:p.Arg312=
NM_001346091.1:c.611G=	NP_001333020.1:p.Arg204=
NM_001346091.2:c.611G=	NP_001333020.1:p.Arg204=
NM_001346092.1:c.476G=	NP_001333021.1:p.Arg159=
NM_001346092.2:c.476G=	NP_001333021.1:p.Arg159=
NR_144351.1:n.1164G=
NR_144351.2:n.1123G=
ENST00000162749.6:c.935G=	ENSP00000162749.2:p.Arg312=
ENST00000366159.9:n.2036G=
ENST00000437813.8:c.*396G=	ENSP00000513672.1:n.*396G=
ENST00000440083.7:c.1154G=	ENSP00000413224.3:p.Arg385=
ENST00000534885.5:c.*412G=	ENSP00000441803.1:n.*412G=
ENST00000535958.2:c.*762G=	ENSP00000513673.1:n.*762G=
ENST00000536717.5:n.839G=
ENST00000537842.5:n.373-1G=
ENST00000540022.5:c.806G=	ENSP00000438343.1:p.Arg269=
ENST00000543359.5:n.347G=
ENST00000543995.5:c.*522G=	ENSP00000442405.1:n.*522G=
ENST00000698337.1:n.896G=
ENST00000698338.1:n.1549G=
ENST00000698339.1:c.*430G=	ENSP00000513670.1:n.*430G=
ENST00000698340.1:c.*174G=	ENSP00000513671.1:n.*174G=