Canonical Allele Identifier: CA2617250980

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330827-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330827A>C , CM000674.2:g.6330827A>C	GRCh38
NC_000012.11:g.6439993A>C , CM000674.1:g.6439993A>C	GRCh37
NC_000012.10:g.6310254A>C	NCBI36
NG_007506.1:g.16269T>G , LRG_193:g.16269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+26T>G
ENST00000437813.8:c.*86+26T>G	ENSP00000513672.1:n.*86+26T>G
ENST00000440083.7:c.844+26T>G	ENSP00000413224.3:n.844+26T>G
ENST00000535038.2:n.807+26T>G
ENST00000535958.2:c.*452+26T>G	ENSP00000513673.1:n.*452+26T>G
ENST00000698337.1:n.500T>G
ENST00000698338.1:n.924T>G
ENST00000698339.1:c.*120+26T>G	ENSP00000513670.1:n.*120+26T>G
ENST00000698340.1:c.552-116T>G	ENSP00000513671.1:n.552-116T>G
ENST00000162749.7:c.625+26T>G MANE Select	ENSP00000162749.2:n.625+26T>G
ENST00000162749.6:c.625+26T>G	ENSP00000162749.2:n.625+26T>G
ENST00000534885.5:c.*102+26T>G	ENSP00000441803.1:n.*102+26T>G
ENST00000535038.1:n.321T>G
ENST00000536717.5:n.529+26T>G
ENST00000537842.5:n.229+26T>G
ENST00000539372.5:c.625+26T>G	ENSP00000442059.1:n.625+26T>G
ENST00000540022.5:c.496+26T>G	ENSP00000438343.1:n.496+26T>G
ENST00000543359.5:n.38-116T>G
ENST00000543995.5:c.*212+26T>G	ENSP00000442405.1:n.*212+26T>G
NM_001065.3:c.625+26T>G , LRG_193t1:c.625+26T>G	NP_001056.1:n.625+26T>G
NM_001346091.1:c.301+26T>G	NP_001333020.1:n.301+26T>G
NM_001346092.1:c.166+26T>G	NP_001333021.1:n.166+26T>G
NR_144351.1:n.855-116T>G
NM_001065.4:c.625+26T>G MANE Select	NP_001056.1:n.625+26T>G
NM_001346091.2:c.301+26T>G	NP_001333020.1:n.301+26T>G
NM_001346092.2:c.166+26T>G	NP_001333021.1:n.166+26T>G
NR_144351.2:n.814-116T>G