Canonical Allele Identifier: CA2014022971
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6329924C= , CM000674.2:g.6329924C= GRCh38
NC_000012.11:g.6439090C= , CM000674.1:g.6439090C= GRCh37
NC_000012.10:g.6309351C= NCBI36
NG_007506.1:g.17172G= , LRG_193:g.17172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.2012G=
ENST00000437813.8:c.*372G= ENSP00000513672.1:n.*372G=
ENST00000440083.7:c.1130G= ENSP00000413224.3:p.Cys377=
ENST00000535958.2:c.*738G= ENSP00000513673.1:n.*738G=
ENST00000698337.1:n.872G=
ENST00000698338.1:n.1525G=
ENST00000698339.1:c.*406G= ENSP00000513670.1:n.*406G=
ENST00000698340.1:c.*150G= ENSP00000513671.1:n.*150G=
ENST00000162749.7:c.911G= MANE Select ENSP00000162749.2:p.Cys304=
ENST00000162749.6:c.911G= ENSP00000162749.2:p.Cys304=
ENST00000534885.5:c.*388G= ENSP00000441803.1:n.*388G=
ENST00000536717.5:n.815G=
ENST00000537842.5:n.373-25G=
ENST00000540022.5:c.782G= ENSP00000438343.1:p.Cys261=
ENST00000543359.5:n.323G=
ENST00000543995.5:c.*498G= ENSP00000442405.1:n.*498G=
NM_001065.3:c.911G= , LRG_193t1:c.911G= NP_001056.1:p.Cys304=
NM_001346091.1:c.587G= NP_001333020.1:p.Cys196=
NM_001346092.1:c.452G= NP_001333021.1:p.Cys151=
NR_144351.1:n.1140G=
NM_001065.4:c.911G= MANE Select NP_001056.1:p.Cys304=
NM_001346091.2:c.587G= NP_001333020.1:p.Cys196=
NM_001346092.2:c.452G= NP_001333021.1:p.Cys151=
NR_144351.2:n.1099G=