Canonical Allele Identifier: CA383545608

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329798T>C , CM000674.2:g.6329798T>C	GRCh38
NC_000012.11:g.6438964T>C , CM000674.1:g.6438964T>C	GRCh37
NC_000012.10:g.6309225T>C	NCBI36
NG_007506.1:g.17298A>G , LRG_193:g.17298A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.1037A>G MANE Select	NP_001056.1:p.His346Arg
ENST00000162749.7:c.1037A>G MANE Select	ENSP00000162749.2:p.His346Arg
NM_001065.3:c.1037A>G , LRG_193t1:c.1037A>G	NP_001056.1:p.His346Arg
NM_001346091.1:c.713A>G	NP_001333020.1:p.His238Arg
NM_001346091.2:c.713A>G	NP_001333020.1:p.His238Arg
NM_001346092.1:c.578A>G	NP_001333021.1:p.His193Arg
NM_001346092.2:c.578A>G	NP_001333021.1:p.His193Arg
NR_144351.1:n.1266A>G
NR_144351.2:n.1225A>G
ENST00000162749.6:c.1037A>G	ENSP00000162749.2:p.His346Arg
ENST00000366159.9:n.2138A>G
ENST00000437813.8:c.*498A>G	ENSP00000513672.1:n.*498A>G
ENST00000440083.7:c.1256A>G	ENSP00000413224.3:p.His419Arg
ENST00000534885.5:c.*514A>G	ENSP00000441803.1:n.*514A>G
ENST00000535958.2:c.*864A>G	ENSP00000513673.1:n.*864A>G
ENST00000536717.5:n.941A>G
ENST00000540022.5:c.908A>G	ENSP00000438343.1:p.His303Arg
ENST00000543359.5:n.449A>G
ENST00000543995.5:c.*624A>G	ENSP00000442405.1:n.*624A>G
ENST00000698337.1:n.998A>G
ENST00000698338.1:n.1651A>G
ENST00000698339.1:c.*532A>G	ENSP00000513670.1:n.*532A>G
ENST00000698340.1:c.*276A>G	ENSP00000513671.1:n.*276A>G