Canonical Allele Identifier: CA2695215993
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333783_6333806del , CM000674.2:g.6333783_6333806del GRCh38
NC_000012.11:g.6442949_6442972del , CM000674.1:g.6442949_6442972del GRCh37
NC_000012.10:g.6313210_6313233del NCBI36
NG_007506.1:g.13292_13315del , LRG_193:g.13292_13315del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.289_312del
ENST00000437813.8:c.255_278del ENSP00000513672.1:p.Ser86_Glu93del
ENST00000440083.7:c.255_278del ENSP00000413224.3:p.Ser86_Glu93del
ENST00000535958.2:c.*82_*105del ENSP00000513673.1:n.*82_*105del
ENST00000698339.1:c.255_278del ENSP00000513670.1:p.Ser86_Glu93del
ENST00000698340.1:c.255_278del ENSP00000513671.1:p.Ser86_Glu93del
ENST00000162749.7:c.255_278del MANE Select ENSP00000162749.2:p.Ser86_Glu93del
ENST00000162749.6:c.255_278del ENSP00000162749.2:p.Ser86_Glu93del
ENST00000366159.8:c.255_278del ENSP00000380389.3:p.Ser86_Glu93del
ENST00000437813.7:n.216_239del
ENST00000440083.6:c.255_278del ENSP00000413224.2:p.Ser86_Glu93del
ENST00000534885.5:c.101_124del ENSP00000441803.1:p.Arg34_Gln41del
ENST00000535958.1:n.501_524del
ENST00000536194.1:c.228_251del ENSP00000442919.1:p.Ser77_Glu84del
ENST00000539372.5:c.255_278del ENSP00000442059.1:p.Ser86_Glu93del
ENST00000540022.5:c.194-288_194-265del ENSP00000438343.1:n.194-288_194-265del
ENST00000543048.5:c.214+41_214+64del ENSP00000439981.1:n.214+41_214+64del
ENST00000543995.5:c.193+287_193+310del ENSP00000442405.1:n.193+287_193+310del
NM_001065.3:c.255_278del , LRG_193t1:c.255_278del NP_001056.1:p.Ser86_Glu93del
NM_001346091.1:c.-70_-47del NP_001333020.1:n.-70_-47del
NM_001346092.1:c.-323_-300del NP_001333021.1:n.-323_-300del
NR_144351.1:n.558_581del
NM_001065.4:c.255_278del MANE Select NP_001056.1:p.Ser86_Glu93del
NM_001346091.2:c.-70_-47del NP_001333020.1:n.-70_-47del
NM_001346092.2:c.-323_-300del NP_001333021.1:n.-323_-300del
NR_144351.2:n.517_540del