Canonical Allele Identifier: CA2575003661
Gene: TNFRSF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6330848_6330850del , CM000674.2:g.6330848_6330850del GRCh38
NC_000012.11:g.6440014_6440016del , CM000674.1:g.6440014_6440016del GRCh37
NC_000012.10:g.6310275_6310277del NCBI36
NG_007506.1:g.16249_16251del , LRG_193:g.16249_16251del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.1726+6_1726+8del
ENST00000437813.8:c.*86+6_*86+8del ENSP00000513672.1:n.*86+6_*86+8del
ENST00000440083.7:c.844+6_844+8del ENSP00000413224.3:n.844+6_844+8del
ENST00000535038.2:n.807+6_807+8del
ENST00000535958.2:c.*452+6_*452+8del ENSP00000513673.1:n.*452+6_*452+8del
ENST00000698337.1:n.480_482del
ENST00000698338.1:n.904_906del
ENST00000698339.1:c.*120+6_*120+8del ENSP00000513670.1:n.*120+6_*120+8del
ENST00000698340.1:c.552-136_552-134del ENSP00000513671.1:n.552-136_552-134del
ENST00000162749.7:c.625+6_625+8del MANE Select ENSP00000162749.2:n.625+6_625+8del
ENST00000162749.6:c.625+6_625+8del ENSP00000162749.2:n.625+6_625+8del
ENST00000534885.5:c.*102+6_*102+8del ENSP00000441803.1:n.*102+6_*102+8del
ENST00000535038.1:n.301_303del
ENST00000536717.5:n.529+6_529+8del
ENST00000537842.5:n.229+6_229+8del
ENST00000539372.5:c.625+6_625+8del ENSP00000442059.1:n.625+6_625+8del
ENST00000540022.5:c.496+6_496+8del ENSP00000438343.1:n.496+6_496+8del
ENST00000543359.5:n.38-136_38-134del
ENST00000543995.5:c.*212+6_*212+8del ENSP00000442405.1:n.*212+6_*212+8del
NM_001065.3:c.625+6_625+8del , LRG_193t1:c.625+6_625+8del NP_001056.1:n.625+6_625+8del
NM_001346091.1:c.301+6_301+8del NP_001333020.1:n.301+6_301+8del
NM_001346092.1:c.166+6_166+8del NP_001333021.1:n.166+6_166+8del
NR_144351.1:n.855-136_855-134del
NM_001065.4:c.625+6_625+8del MANE Select NP_001056.1:n.625+6_625+8del
NM_001346091.2:c.301+6_301+8del NP_001333020.1:n.301+6_301+8del
NM_001346092.2:c.166+6_166+8del NP_001333021.1:n.166+6_166+8del
NR_144351.2:n.814-136_814-134del