Canonical Allele Identifier: CA2725528858

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs2136817185

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330587C>G , CM000674.2:g.6330587C>G	GRCh38
NC_000012.11:g.6439753C>G , CM000674.1:g.6439753C>G	GRCh37
NC_000012.10:g.6310014C>G	NCBI36
NG_007506.1:g.16509G>C , LRG_193:g.16509G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1840+11G>C
ENST00000437813.8:c.*200+11G>C	ENSP00000513672.1:n.*200+11G>C
ENST00000440083.7:c.958+11G>C	ENSP00000413224.3:n.958+11G>C
ENST00000535038.2:n.921+11G>C
ENST00000535958.2:c.*566+11G>C	ENSP00000513673.1:n.*566+11G>C
ENST00000698337.1:n.729+11G>C
ENST00000698338.1:n.1153+11G>C
ENST00000698339.1:c.*234+11G>C	ENSP00000513670.1:n.*234+11G>C
ENST00000698340.1:c.665+11G>C	ENSP00000513671.1:n.665+11G>C
ENST00000162749.7:c.739+11G>C MANE Select	ENSP00000162749.2:n.739+11G>C
ENST00000162749.6:c.739+11G>C	ENSP00000162749.2:n.739+11G>C
ENST00000534885.5:c.*216+11G>C	ENSP00000441803.1:n.*216+11G>C
ENST00000535038.1:n.550+11G>C
ENST00000536717.5:n.643+11G>C
ENST00000537842.5:n.343+11G>C
ENST00000539372.5:c.750G>C	ENSP00000442059.1:p.Gly250=
ENST00000540022.5:c.610+11G>C	ENSP00000438343.1:n.610+11G>C
ENST00000543359.5:n.151+11G>C
ENST00000543995.5:c.*326+11G>C	ENSP00000442405.1:n.*326+11G>C
NM_001065.3:c.739+11G>C , LRG_193t1:c.739+11G>C	NP_001056.1:n.739+11G>C
NM_001346091.1:c.415+11G>C	NP_001333020.1:n.415+11G>C
NM_001346092.1:c.280+11G>C	NP_001333021.1:n.280+11G>C
NR_144351.1:n.968+11G>C
NM_001065.4:c.739+11G>C MANE Select	NP_001056.1:n.739+11G>C
NM_001346091.2:c.415+11G>C	NP_001333020.1:n.415+11G>C
NM_001346092.2:c.280+11G>C	NP_001333021.1:n.280+11G>C
NR_144351.2:n.927+11G>C