Canonical Allele Identifier: CA2575003640
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6330785G>T , CM000674.2:g.6330785G>T GRCh38
NC_000012.11:g.6439951G>T , CM000674.1:g.6439951G>T GRCh37
NC_000012.10:g.6310212G>T NCBI36
NG_007506.1:g.16311C>A , LRG_193:g.16311C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.1726+68C>A
ENST00000437813.8:c.*86+68C>A ENSP00000513672.1:n.*86+68C>A
ENST00000440083.7:c.844+68C>A ENSP00000413224.3:n.844+68C>A
ENST00000535038.2:n.807+68C>A
ENST00000535958.2:c.*452+68C>A ENSP00000513673.1:n.*452+68C>A
ENST00000698337.1:n.542C>A
ENST00000698338.1:n.966C>A
ENST00000698339.1:c.*120+68C>A ENSP00000513670.1:n.*120+68C>A
ENST00000698340.1:c.552-74C>A ENSP00000513671.1:n.552-74C>A
ENST00000162749.7:c.625+68C>A MANE Select ENSP00000162749.2:n.625+68C>A
ENST00000162749.6:c.625+68C>A ENSP00000162749.2:n.625+68C>A
ENST00000534885.5:c.*102+68C>A ENSP00000441803.1:n.*102+68C>A
ENST00000535038.1:n.363C>A
ENST00000536717.5:n.529+68C>A
ENST00000537842.5:n.229+68C>A
ENST00000539372.5:c.625+68C>A ENSP00000442059.1:n.625+68C>A
ENST00000540022.5:c.496+68C>A ENSP00000438343.1:n.496+68C>A
ENST00000543359.5:n.38-74C>A
ENST00000543995.5:c.*212+68C>A ENSP00000442405.1:n.*212+68C>A
NM_001065.3:c.625+68C>A , LRG_193t1:c.625+68C>A NP_001056.1:n.625+68C>A
NM_001346091.1:c.301+68C>A NP_001333020.1:n.301+68C>A
NM_001346092.1:c.166+68C>A NP_001333021.1:n.166+68C>A
NR_144351.1:n.855-74C>A
NM_001065.4:c.625+68C>A MANE Select NP_001056.1:n.625+68C>A
NM_001346091.2:c.301+68C>A NP_001333020.1:n.301+68C>A
NM_001346092.2:c.166+68C>A NP_001333021.1:n.166+68C>A
NR_144351.2:n.814-74C>A