Canonical Allele Identifier: CA2014022728

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329816T= , CM000674.2:g.6329816T=	GRCh38
NC_000012.11:g.6438982T= , CM000674.1:g.6438982T=	GRCh37
NC_000012.10:g.6309243T=	NCBI36
NG_007506.1:g.17280A= , LRG_193:g.17280A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2120A=
ENST00000437813.8:c.*480A=	ENSP00000513672.1:n.*480A=
ENST00000440083.7:c.1238A=	ENSP00000413224.3:p.Lys413=
ENST00000535958.2:c.*846A=	ENSP00000513673.1:n.*846A=
ENST00000698337.1:n.980A=
ENST00000698338.1:n.1633A=
ENST00000698339.1:c.*514A=	ENSP00000513670.1:n.*514A=
ENST00000698340.1:c.*258A=	ENSP00000513671.1:n.*258A=
ENST00000162749.7:c.1019A= MANE Select	ENSP00000162749.2:p.Lys340=
ENST00000162749.6:c.1019A=	ENSP00000162749.2:p.Lys340=
ENST00000534885.5:c.*496A=	ENSP00000441803.1:n.*496A=
ENST00000536717.5:n.923A=
ENST00000540022.5:c.890A=	ENSP00000438343.1:p.Lys297=
ENST00000543359.5:n.431A=
ENST00000543995.5:c.*606A=	ENSP00000442405.1:n.*606A=
NM_001065.3:c.1019A= , LRG_193t1:c.1019A=	NP_001056.1:p.Lys340=
NM_001346091.1:c.695A=	NP_001333020.1:p.Lys232=
NM_001346092.1:c.560A=	NP_001333021.1:p.Lys187=
NR_144351.1:n.1248A=
NM_001065.4:c.1019A= MANE Select	NP_001056.1:p.Lys340=
NM_001346091.2:c.695A=	NP_001333020.1:p.Lys232=
NM_001346092.2:c.560A=	NP_001333021.1:p.Lys187=
NR_144351.2:n.1207A=