Canonical Allele Identifier: CA2014024023

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330676C= , CM000674.2:g.6330676C=	GRCh38
NC_000012.11:g.6439842C= , CM000674.1:g.6439842C=	GRCh37
NC_000012.10:g.6310103C=	NCBI36
NG_007506.1:g.16420G= , LRG_193:g.16420G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1762G=
ENST00000437813.8:c.*122G=	ENSP00000513672.1:n.*122G=
ENST00000440083.7:c.880G=	ENSP00000413224.3:p.Gly294=
ENST00000535038.2:n.843G=
ENST00000535958.2:c.*488G=	ENSP00000513673.1:n.*488G=
ENST00000698337.1:n.651G=
ENST00000698338.1:n.1075G=
ENST00000698339.1:c.*156G=	ENSP00000513670.1:n.*156G=
ENST00000698340.1:c.587G=	ENSP00000513671.1:p.Trp196=
ENST00000162749.7:c.661G= MANE Select	ENSP00000162749.2:p.Gly221=
ENST00000162749.6:c.661G=	ENSP00000162749.2:p.Gly221=
ENST00000534885.5:c.*138G=	ENSP00000441803.1:n.*138G=
ENST00000535038.1:n.472G=
ENST00000536717.5:n.565G=
ENST00000537842.5:n.265G=
ENST00000539372.5:c.661G=	ENSP00000442059.1:p.Gly221=
ENST00000540022.5:c.532G=	ENSP00000438343.1:p.Gly178=
ENST00000543359.5:n.73G=
ENST00000543995.5:c.*248G=	ENSP00000442405.1:n.*248G=
NM_001065.3:c.661G= , LRG_193t1:c.661G=	NP_001056.1:p.Gly221=
NM_001346091.1:c.337G=	NP_001333020.1:p.Gly113=
NM_001346092.1:c.202G=	NP_001333021.1:p.Gly68=
NR_144351.1:n.890G=
NM_001065.4:c.661G= MANE Select	NP_001056.1:p.Gly221=
NM_001346091.2:c.337G=	NP_001333020.1:p.Gly113=
NM_001346092.2:c.202G=	NP_001333021.1:p.Gly68=
NR_144351.2:n.849G=