Canonical Allele Identifier: CA2580601251

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330843T>G , CM000674.2:g.6330843T>G	GRCh38
NC_000012.11:g.6440009T>G , CM000674.1:g.6440009T>G	GRCh37
NC_000012.10:g.6310270T>G	NCBI36
NG_007506.1:g.16253A>C , LRG_193:g.16253A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+10A>C
ENST00000437813.8:c.*86+10A>C	ENSP00000513672.1:n.*86+10A>C
ENST00000440083.7:c.844+10A>C	ENSP00000413224.3:n.844+10A>C
ENST00000535038.2:n.807+10A>C
ENST00000535958.2:c.*452+10A>C	ENSP00000513673.1:n.*452+10A>C
ENST00000698337.1:n.484A>C
ENST00000698338.1:n.908A>C
ENST00000698339.1:c.*120+10A>C	ENSP00000513670.1:n.*120+10A>C
ENST00000698340.1:c.552-132A>C	ENSP00000513671.1:n.552-132A>C
ENST00000162749.7:c.625+10A>C MANE Select	ENSP00000162749.2:n.625+10A>C
ENST00000162749.6:c.625+10A>C	ENSP00000162749.2:n.625+10A>C
ENST00000534885.5:c.*102+10A>C	ENSP00000441803.1:n.*102+10A>C
ENST00000535038.1:n.305A>C
ENST00000536717.5:n.529+10A>C
ENST00000537842.5:n.229+10A>C
ENST00000539372.5:c.625+10A>C	ENSP00000442059.1:n.625+10A>C
ENST00000540022.5:c.496+10A>C	ENSP00000438343.1:n.496+10A>C
ENST00000543359.5:n.38-132A>C
ENST00000543995.5:c.*212+10A>C	ENSP00000442405.1:n.*212+10A>C
NM_001065.3:c.625+10A>C , LRG_193t1:c.625+10A>C	NP_001056.1:n.625+10A>C
NM_001346091.1:c.301+10A>C	NP_001333020.1:n.301+10A>C
NM_001346092.1:c.166+10A>C	NP_001333021.1:n.166+10A>C
NR_144351.1:n.855-132A>C
NM_001065.4:c.625+10A>C MANE Select	NP_001056.1:n.625+10A>C
NM_001346091.2:c.301+10A>C	NP_001333020.1:n.301+10A>C
NM_001346092.2:c.166+10A>C	NP_001333021.1:n.166+10A>C
NR_144351.2:n.814-132A>C