Canonical Allele Identifier: CA2014022579

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329711G= , CM000674.2:g.6329711G=	GRCh38
NC_000012.11:g.6438877G= , CM000674.1:g.6438877G=	GRCh37
NC_000012.10:g.6309138G=	NCBI36
NG_007506.1:g.17385C= , LRG_193:g.17385C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2158+67C=
ENST00000437813.8:c.*518+67C=	ENSP00000513672.1:n.*518+67C=
ENST00000440083.7:c.1276+67C=	ENSP00000413224.3:n.1276+67C=
ENST00000535958.2:c.*884+67C=	ENSP00000513673.1:n.*884+67C=
ENST00000698337.1:n.1018+67C=
ENST00000698338.1:n.1671+67C=
ENST00000698339.1:c.*552+67C=	ENSP00000513670.1:n.*552+67C=
ENST00000698340.1:c.*296+67C=	ENSP00000513671.1:n.*296+67C=
ENST00000162749.7:c.1057+67C= MANE Select	ENSP00000162749.2:n.1057+67C=
ENST00000162749.6:c.1057+67C=	ENSP00000162749.2:n.1057+67C=
ENST00000534885.5:c.*534+67C=	ENSP00000441803.1:n.*534+67C=
ENST00000536717.5:n.961+67C=
ENST00000540022.5:c.928+67C=	ENSP00000438343.1:n.928+67C=
ENST00000543359.5:n.469+67C=
ENST00000543995.5:c.*644+67C=	ENSP00000442405.1:n.*644+67C=
NM_001065.3:c.1057+67C= , LRG_193t1:c.1057+67C=	NP_001056.1:n.1057+67C=
NM_001346091.1:c.733+67C=	NP_001333020.1:n.733+67C=
NM_001346092.1:c.598+67C=	NP_001333021.1:n.598+67C=
NR_144351.1:n.1286+67C=
NM_001065.4:c.1057+67C= MANE Select	NP_001056.1:n.1057+67C=
NM_001346091.2:c.733+67C=	NP_001333020.1:n.733+67C=
NM_001346092.2:c.598+67C=	NP_001333021.1:n.598+67C=
NR_144351.2:n.1245+67C=