Canonical Allele Identifier: CA2555094142

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330639_6330640insAG , CM000674.2:g.6330639_6330640insAG	GRCh38
NC_000012.11:g.6439805_6439806insAG , CM000674.1:g.6439805_6439806insAG	GRCh37
NC_000012.10:g.6310066_6310067insAG	NCBI36
NG_007506.1:g.16456_16457insCT , LRG_193:g.16456_16457insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1798_1799insCT
ENST00000437813.8:c.*158_*159insCT	ENSP00000513672.1:n.*158_*159insCT
ENST00000440083.7:c.916_917insCT	ENSP00000413224.3:p.Met306ThrfsTer?
ENST00000535038.2:n.879_880insCT
ENST00000535958.2:c.*524_*525insCT	ENSP00000513673.1:n.*524_*525insCT
ENST00000698337.1:n.687_688insCT
ENST00000698338.1:n.1111_1112insCT
ENST00000698339.1:c.*192_*193insCT	ENSP00000513670.1:n.*192_*193insCT
ENST00000698340.1:c.623_624insCT	ENSP00000513671.1:p.Val209LeufsTer?
ENST00000162749.7:c.697_698insCT MANE Select	ENSP00000162749.2:p.Met233ThrfsTer?
ENST00000162749.6:c.697_698insCT	ENSP00000162749.2:p.Met233ThrfsTer?
ENST00000534885.5:c.*174_*175insCT	ENSP00000441803.1:n.*174_*175insCT
ENST00000535038.1:n.508_509insCT
ENST00000536717.5:n.601_602insCT
ENST00000537842.5:n.301_302insCT
ENST00000539372.5:c.697_698insCT	ENSP00000442059.1:p.Met233ThrfsTer?
ENST00000540022.5:c.568_569insCT	ENSP00000438343.1:p.Met190ThrfsTer?
ENST00000543359.5:n.109_110insCT
ENST00000543995.5:c.*284_*285insCT	ENSP00000442405.1:n.*284_*285insCT
NM_001065.3:c.697_698insCT , LRG_193t1:c.697_698insCT	NP_001056.1:p.Met233ThrfsTer?
NM_001346091.1:c.373_374insCT	NP_001333020.1:p.Met125ThrfsTer?
NM_001346092.1:c.238_239insCT	NP_001333021.1:p.Met80ThrfsTer?
NR_144351.1:n.926_927insCT
NM_001065.4:c.697_698insCT MANE Select	NP_001056.1:p.Met233ThrfsTer?
NM_001346091.2:c.373_374insCT	NP_001333020.1:p.Met125ThrfsTer?
NM_001346092.2:c.238_239insCT	NP_001333021.1:p.Met80ThrfsTer?
NR_144351.2:n.885_886insCT