Canonical Allele Identifier: CA2695215991

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333441_6333446del , CM000674.2:g.6333441_6333446del	GRCh38
NC_000012.11:g.6442607_6442612del , CM000674.1:g.6442607_6442612del	GRCh37
NC_000012.10:g.6312868_6312873del	NCBI36
NG_007506.1:g.13651_13656del , LRG_193:g.13651_13656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.428_433del
ENST00000437813.8:c.394_399del	ENSP00000513672.1:p.Tyr132_Arg133del
ENST00000440083.7:c.394_399del	ENSP00000413224.3:p.Tyr132_Arg133del
ENST00000535958.2:c.*221_*226del	ENSP00000513673.1:n.*221_*226del
ENST00000698339.1:c.394_399del	ENSP00000513670.1:p.Tyr132_Arg133del
ENST00000698340.1:c.394_399del	ENSP00000513671.1:p.Tyr132_Arg133del
ENST00000162749.7:c.394_399del MANE Select	ENSP00000162749.2:p.Tyr132_Arg133del
ENST00000162749.6:c.394_399del	ENSP00000162749.2:p.Tyr132_Arg133del
ENST00000366159.8:c.394_399del	ENSP00000380389.3:p.Tyr132_Arg133del
ENST00000437813.7:n.355_360del
ENST00000440083.6:c.394_399del	ENSP00000413224.2:p.Tyr132_Arg133del
ENST00000534885.5:c.240_245del	ENSP00000441803.1:p.Thr81_Gly82del
ENST00000539372.5:c.394_399del	ENSP00000442059.1:p.Tyr132_Arg133del
ENST00000540022.5:c.265_270del	ENSP00000438343.1:p.Tyr89_Arg90del
ENST00000543048.5:c.*5_*10del	ENSP00000439981.1:n.*5_*10del
ENST00000543995.5:c.200_205del	ENSP00000442405.1:p.Val67_Pro68del
NM_001065.3:c.394_399del , LRG_193t1:c.394_399del	NP_001056.1:p.Tyr132_Arg133del
NM_001346091.1:c.70_75del	NP_001333020.1:p.Tyr24_Arg25del
NM_001346092.1:c.-184_-179del	NP_001333021.1:n.-184_-179del
NR_144351.1:n.697_702del
NM_001065.4:c.394_399del MANE Select	NP_001056.1:p.Tyr132_Arg133del
NM_001346091.2:c.70_75del	NP_001333020.1:p.Tyr24_Arg25del
NM_001346092.2:c.-184_-179del	NP_001333021.1:n.-184_-179del
NR_144351.2:n.656_661del