Canonical Allele Identifier: CA10577453

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330029G>C , CM000674.2:g.6330029G>C	GRCh38
NC_000012.11:g.6439195G>C , CM000674.1:g.6439195G>C	GRCh37
NC_000012.10:g.6309456G>C	NCBI36
NG_007506.1:g.17067C>G , LRG_193:g.17067C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1907C>G
ENST00000437813.8:c.*267C>G	ENSP00000513672.1:n.*267C>G
ENST00000440083.7:c.1025C>G	ENSP00000413224.3:p.Pro342Arg
ENST00000535038.2:n.1188C>G
ENST00000535958.2:c.*633C>G	ENSP00000513673.1:n.*633C>G
ENST00000698337.1:n.767C>G
ENST00000698338.1:n.1420C>G
ENST00000698339.1:c.*301C>G	ENSP00000513670.1:n.*301C>G
ENST00000698340.1:c.*45C>G	ENSP00000513671.1:n.*45C>G
ENST00000162749.7:c.806C>G MANE Select	ENSP00000162749.2:p.Pro269Arg
ENST00000162749.6:c.806C>G	ENSP00000162749.2:p.Pro269Arg
ENST00000534885.5:c.*283C>G	ENSP00000441803.1:n.*283C>G
ENST00000536717.5:n.710C>G
ENST00000537842.5:n.373-130C>G
ENST00000540022.5:c.677C>G	ENSP00000438343.1:p.Pro226Arg
ENST00000543359.5:n.218C>G
ENST00000543995.5:c.*393C>G	ENSP00000442405.1:n.*393C>G
NM_001065.3:c.806C>G , LRG_193t1:c.806C>G	NP_001056.1:p.Pro269Arg
NM_001346091.1:c.482C>G	NP_001333020.1:p.Pro161Arg
NM_001346092.1:c.347C>G	NP_001333021.1:p.Pro116Arg
NR_144351.1:n.1035C>G
NM_001065.4:c.806C>G MANE Select	NP_001056.1:p.Pro269Arg
NM_001346091.2:c.482C>G	NP_001333020.1:p.Pro161Arg
NM_001346092.2:c.347C>G	NP_001333021.1:p.Pro116Arg
NR_144351.2:n.994C>G