Canonical Allele Identifier: CA2014022548

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329689_6329714delinsCCGCCTCTCGTGGTCCCCTCTGGGAG , CM000674.2:g.6329689_6329714delinsCCGCCTCTCGTGGTCCCCTCTGGGAG	GRCh38
NC_000012.11:g.6438855_6438880delinsCCGCCTCTCGTGGTCCCCTCTGGGAG , CM000674.1:g.6438855_6438880delinsCCGCCTCTCGTGGTCCCCTCTGGGAG	GRCh37
NC_000012.10:g.6309116_6309141delinsCCGCCTCTCGTGGTCCCCTCTGGGAG	NCBI36
NG_007506.1:g.17382_17407delinsCTCCCAGAGGGGACCACGAGAGGCGG , LRG_193:g.17382_17407delinsCTCCCAGAGGGGACCACGAGAGGCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2158+64_2159-67delinsCTCCCAGAGGGGACCACGAGAGGCGG
ENST00000437813.8:c.*518+64_*519-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000513672.1:n.*518+64_*519-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000440083.7:c.1276+64_1277-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000413224.3:n.1276+64_1277-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000535958.2:c.*884+64_*885-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000513673.1:n.*884+64_*885-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000698337.1:n.1018+64_1019-67delinsCTCCCAGAGGGGACCACGAGAGGCGG
ENST00000698338.1:n.1671+64_1672-67delinsCTCCCAGAGGGGACCACGAGAGGCGG
ENST00000698339.1:c.*552+64_*553-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000513670.1:n.*552+64_*553-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000698340.1:c.*296+64_*297-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000513671.1:n.*296+64_*297-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000162749.7:c.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAGAGGCGG MANE Select	ENSP00000162749.2:n.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000162749.6:c.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000162749.2:n.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000534885.5:c.*534+64_*535-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000441803.1:n.*534+64_*535-67delinsCTCCCAGAGGGGACCACGAG...
ENST00000536717.5:n.961+64_962-67delinsCTCCCAGAGGGGACCACGAGAGGCGG
ENST00000540022.5:c.928+64_929-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000438343.1:n.928+64_929-67delinsCTCCCAGAGGGGACCACGAGAG...
ENST00000543359.5:n.469+64_470-67delinsCTCCCAGAGGGGACCACGAGAGGCGG
ENST00000543995.5:c.*644+64_*645-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	ENSP00000442405.1:n.*644+64_*645-67delinsCTCCCAGAGGGGACCACGAG...
NM_001065.3:c.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAGAGGCGG , LRG_193t1:c.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	NP_001056.1:n.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAGAGGCGG...
NM_001346091.1:c.733+64_734-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	NP_001333020.1:n.733+64_734-67delinsCTCCCAGAGGGGACCACGAGAGGCG...
NM_001346092.1:c.598+64_599-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	NP_001333021.1:n.598+64_599-67delinsCTCCCAGAGGGGACCACGAGAGGCG...
NR_144351.1:n.1286+64_1287-67delinsCTCCCAGAGGGGACCACGAGAGGCGG
NM_001065.4:c.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAGAGGCGG MANE Select	NP_001056.1:n.1057+64_1058-67delinsCTCCCAGAGGGGACCACGAGAGGCGG...
NM_001346091.2:c.733+64_734-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	NP_001333020.1:n.733+64_734-67delinsCTCCCAGAGGGGACCACGAGAGGCG...
NM_001346092.2:c.598+64_599-67delinsCTCCCAGAGGGGACCACGAGAGGCGG	NP_001333021.1:n.598+64_599-67delinsCTCCCAGAGGGGACCACGAGAGGCG...
NR_144351.2:n.1245+64_1246-67delinsCTCCCAGAGGGGACCACGAGAGGCGG