Canonical Allele Identifier: CA2014026005

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333312_6333313delinsAG , CM000674.2:g.6333312_6333313delinsAG	GRCh38
NC_000012.11:g.6442478_6442479delinsAG , CM000674.1:g.6442478_6442479delinsAG	GRCh37
NC_000012.10:g.6312739_6312740delinsAG	NCBI36
NG_007506.1:g.13783_13784delinsCT , LRG_193:g.13783_13784delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.506+54_506+55delinsCT
ENST00000437813.8:c.472+54_472+55delinsCT	ENSP00000513672.1:n.472+54_472+55delinsCT
ENST00000440083.7:c.526_527delinsCT	ENSP00000413224.3:p.Leu176=
ENST00000535958.2:c.*299+54_*299+55delinsCT	ENSP00000513673.1:n.*299+54_*299+55delinsCT
ENST00000698339.1:c.472+54_472+55delinsCT	ENSP00000513670.1:n.472+54_472+55delinsCT
ENST00000698340.1:c.472+54_472+55delinsCT	ENSP00000513671.1:n.472+54_472+55delinsCT
ENST00000162749.7:c.472+54_472+55delinsCT MANE Select	ENSP00000162749.2:n.472+54_472+55delinsCT
ENST00000162749.6:c.472+54_472+55delinsCT	ENSP00000162749.2:n.472+54_472+55delinsCT
ENST00000366159.8:c.472+54_472+55delinsCT	ENSP00000380389.3:n.472+54_472+55delinsCT
ENST00000437813.7:n.433+54_433+55delinsCT
ENST00000440083.6:c.526_527delinsCT	ENSP00000413224.2:p.Leu176=
ENST00000534885.5:c.318+54_318+55delinsCT	ENSP00000441803.1:n.318+54_318+55delinsCT
ENST00000537842.5:n.76+54_76+55delinsCT
ENST00000539372.5:c.472+54_472+55delinsCT	ENSP00000442059.1:n.472+54_472+55delinsCT
ENST00000540022.5:c.343+54_343+55delinsCT	ENSP00000438343.1:n.343+54_343+55delinsCT
ENST00000543048.5:c.*83+54_*83+55delinsCT	ENSP00000439981.1:n.*83+54_*83+55delinsCT
ENST00000543995.5:c.*59+54_*59+55delinsCT	ENSP00000442405.1:n.*59+54_*59+55delinsCT
NM_001065.3:c.472+54_472+55delinsCT , LRG_193t1:c.472+54_472+55delinsCT	NP_001056.1:n.472+54_472+55delinsCT
NM_001346091.1:c.148+54_148+55delinsCT	NP_001333020.1:n.148+54_148+55delinsCT
NM_001346092.1:c.-106+54_-106+55delinsCT	NP_001333021.1:n.-106+54_-106+55delinsCT
NR_144351.1:n.775+54_775+55delinsCT
NM_001065.4:c.472+54_472+55delinsCT MANE Select	NP_001056.1:n.472+54_472+55delinsCT
NM_001346091.2:c.148+54_148+55delinsCT	NP_001333020.1:n.148+54_148+55delinsCT
NM_001346092.2:c.-106+54_-106+55delinsCT	NP_001333021.1:n.-106+54_-106+55delinsCT
NR_144351.2:n.734+54_734+55delinsCT