Canonical Allele Identifier: CA2014022741
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6329819T= , CM000674.2:g.6329819T= GRCh38
NC_000012.11:g.6438985T= , CM000674.1:g.6438985T= GRCh37
NC_000012.10:g.6309246T= NCBI36
NG_007506.1:g.17277A= , LRG_193:g.17277A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366159.9:n.2117A=
ENST00000437813.8:c.*477A= ENSP00000513672.1:n.*477A=
ENST00000440083.7:c.1235A= ENSP00000413224.3:p.Gln412=
ENST00000535958.2:c.*843A= ENSP00000513673.1:n.*843A=
ENST00000698337.1:n.977A=
ENST00000698338.1:n.1630A=
ENST00000698339.1:c.*511A= ENSP00000513670.1:n.*511A=
ENST00000698340.1:c.*255A= ENSP00000513671.1:n.*255A=
ENST00000162749.7:c.1016A= MANE Select ENSP00000162749.2:p.Gln339=
ENST00000162749.6:c.1016A= ENSP00000162749.2:p.Gln339=
ENST00000534885.5:c.*493A= ENSP00000441803.1:n.*493A=
ENST00000536717.5:n.920A=
ENST00000540022.5:c.887A= ENSP00000438343.1:p.Gln296=
ENST00000543359.5:n.428A=
ENST00000543995.5:c.*603A= ENSP00000442405.1:n.*603A=
NM_001065.3:c.1016A= , LRG_193t1:c.1016A= NP_001056.1:p.Gln339=
NM_001346091.1:c.692A= NP_001333020.1:p.Gln231=
NM_001346092.1:c.557A= NP_001333021.1:p.Gln186=
NR_144351.1:n.1245A=
NM_001065.4:c.1016A= MANE Select NP_001056.1:p.Gln339=
NM_001346091.2:c.692A= NP_001333020.1:p.Gln231=
NM_001346092.2:c.557A= NP_001333021.1:p.Gln186=
NR_144351.2:n.1204A=