Canonical Allele Identifier: CA6405356

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330051T>C , CM000674.2:g.6330051T>C	GRCh38
NC_000012.11:g.6439217T>C , CM000674.1:g.6439217T>C	GRCh37
NC_000012.10:g.6309478T>C	NCBI36
NG_007506.1:g.17045A>G , LRG_193:g.17045A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.784A>G MANE Select	NP_001056.1:p.Thr262Ala
ENST00000162749.7:c.784A>G MANE Select	ENSP00000162749.2:p.Thr262Ala
NM_001065.3:c.784A>G , LRG_193t1:c.784A>G	NP_001056.1:p.Thr262Ala
NM_001346091.1:c.460A>G	NP_001333020.1:p.Thr154Ala
NM_001346091.2:c.460A>G	NP_001333020.1:p.Thr154Ala
NM_001346092.1:c.325A>G	NP_001333021.1:p.Thr109Ala
NM_001346092.2:c.325A>G	NP_001333021.1:p.Thr109Ala
NR_144351.1:n.1013A>G
NR_144351.2:n.972A>G
ENST00000162749.6:c.784A>G	ENSP00000162749.2:p.Thr262Ala
ENST00000366159.9:n.1885A>G
ENST00000437813.8:c.*245A>G	ENSP00000513672.1:n.*245A>G
ENST00000440083.7:c.1003A>G	ENSP00000413224.3:p.Thr335Ala
ENST00000534885.5:c.*261A>G	ENSP00000441803.1:n.*261A>G
ENST00000535038.2:n.1166A>G
ENST00000535958.2:c.*611A>G	ENSP00000513673.1:n.*611A>G
ENST00000536717.5:n.688A>G
ENST00000537842.5:n.373-152A>G
ENST00000540022.5:c.655A>G	ENSP00000438343.1:p.Thr219Ala
ENST00000543359.5:n.196A>G
ENST00000543995.5:c.*371A>G	ENSP00000442405.1:n.*371A>G
ENST00000698337.1:n.745A>G
ENST00000698338.1:n.1398A>G
ENST00000698339.1:c.*279A>G	ENSP00000513670.1:n.*279A>G
ENST00000698340.1:c.*23A>G	ENSP00000513671.1:n.*23A>G