Canonical Allele Identifier: CA2617251163

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330935-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330935A>G , CM000674.2:g.6330935A>G	GRCh38
NC_000012.11:g.6440101A>G , CM000674.1:g.6440101A>G	GRCh37
NC_000012.10:g.6310362A>G	NCBI36
NG_007506.1:g.16161T>C , LRG_193:g.16161T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1644T>C
ENST00000437813.8:c.*13-9T>C	ENSP00000513672.1:n.*13-9T>C
ENST00000440083.7:c.771-9T>C	ENSP00000413224.3:n.771-9T>C
ENST00000535038.2:n.725T>C
ENST00000535958.2:c.*379-9T>C	ENSP00000513673.1:n.*379-9T>C
ENST00000698337.1:n.392T>C
ENST00000698338.1:n.816T>C
ENST00000698339.1:c.*38T>C	ENSP00000513670.1:n.*38T>C
ENST00000698340.1:c.552-224T>C	ENSP00000513671.1:n.552-224T>C
ENST00000162749.7:c.552-9T>C MANE Select	ENSP00000162749.2:n.552-9T>C
ENST00000162749.6:c.552-9T>C	ENSP00000162749.2:n.552-9T>C
ENST00000534885.5:c.*29-9T>C	ENSP00000441803.1:n.*29-9T>C
ENST00000535038.1:n.213T>C
ENST00000536717.5:n.447T>C
ENST00000537842.5:n.156-9T>C
ENST00000539372.5:c.552-9T>C	ENSP00000442059.1:n.552-9T>C
ENST00000540022.5:c.423-9T>C	ENSP00000438343.1:n.423-9T>C
ENST00000543359.5:n.38-224T>C
ENST00000543995.5:c.*139-9T>C	ENSP00000442405.1:n.*139-9T>C
NM_001065.3:c.552-9T>C , LRG_193t1:c.552-9T>C	NP_001056.1:n.552-9T>C
NM_001346091.1:c.228-9T>C	NP_001333020.1:n.228-9T>C
NM_001346092.1:c.93-9T>C	NP_001333021.1:n.93-9T>C
NR_144351.1:n.855-224T>C
NM_001065.4:c.552-9T>C MANE Select	NP_001056.1:n.552-9T>C
NM_001346091.2:c.228-9T>C	NP_001333020.1:n.228-9T>C
NM_001346092.2:c.93-9T>C	NP_001333021.1:n.93-9T>C
NR_144351.2:n.814-224T>C