Canonical Allele Identifier: CA2617250956
Gene: TNFRSF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6330810_6330813dup , CM000674.2:g.6330810_6330813dup GRCh38
NC_000012.11:g.6439976_6439979dup , CM000674.1:g.6439976_6439979dup GRCh37
NC_000012.10:g.6310237_6310240dup NCBI36
NG_007506.1:g.16286_16289dup , LRG_193:g.16286_16289dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.1726+43_1726+46dup
ENST00000437813.8:c.*86+43_*86+46dup ENSP00000513672.1:n.*86+43_*86+46dup
ENST00000440083.7:c.844+43_844+46dup ENSP00000413224.3:n.844+43_844+46dup
ENST00000535038.2:n.807+43_807+46dup
ENST00000535958.2:c.*452+43_*452+46dup ENSP00000513673.1:n.*452+43_*452+46dup
ENST00000698337.1:n.517_520dup
ENST00000698338.1:n.941_944dup
ENST00000698339.1:c.*120+43_*120+46dup ENSP00000513670.1:n.*120+43_*120+46dup
ENST00000698340.1:c.552-99_552-96dup ENSP00000513671.1:n.552-99_552-96dup
ENST00000162749.7:c.625+43_625+46dup MANE Select ENSP00000162749.2:n.625+43_625+46dup
ENST00000162749.6:c.625+43_625+46dup ENSP00000162749.2:n.625+43_625+46dup
ENST00000534885.5:c.*102+43_*102+46dup ENSP00000441803.1:n.*102+43_*102+46dup
ENST00000535038.1:n.338_341dup
ENST00000536717.5:n.529+43_529+46dup
ENST00000537842.5:n.229+43_229+46dup
ENST00000539372.5:c.625+43_625+46dup ENSP00000442059.1:n.625+43_625+46dup
ENST00000540022.5:c.496+43_496+46dup ENSP00000438343.1:n.496+43_496+46dup
ENST00000543359.5:n.38-99_38-96dup
ENST00000543995.5:c.*212+43_*212+46dup ENSP00000442405.1:n.*212+43_*212+46dup
NM_001065.3:c.625+43_625+46dup , LRG_193t1:c.625+43_625+46dup NP_001056.1:n.625+43_625+46dup
NM_001346091.1:c.301+43_301+46dup NP_001333020.1:n.301+43_301+46dup
NM_001346092.1:c.166+43_166+46dup NP_001333021.1:n.166+43_166+46dup
NR_144351.1:n.855-99_855-96dup
NM_001065.4:c.625+43_625+46dup MANE Select NP_001056.1:n.625+43_625+46dup
NM_001346091.2:c.301+43_301+46dup NP_001333020.1:n.301+43_301+46dup
NM_001346092.2:c.166+43_166+46dup NP_001333021.1:n.166+43_166+46dup
NR_144351.2:n.814-99_814-96dup