Canonical Allele Identifier: CA2725529476

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs2136817876

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330934_6330935del , CM000674.2:g.6330934_6330935del	GRCh38
NC_000012.11:g.6440100_6440101del , CM000674.1:g.6440100_6440101del	GRCh37
NC_000012.10:g.6310361_6310362del	NCBI36
NG_007506.1:g.16161_16162del , LRG_193:g.16161_16162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1644_1645del
ENST00000437813.8:c.*13-9_*13-8del	ENSP00000513672.1:n.*13-9_*13-8del
ENST00000440083.7:c.771-9_771-8del	ENSP00000413224.3:n.771-9_771-8del
ENST00000535038.2:n.725_726del
ENST00000535958.2:c.*379-9_*379-8del	ENSP00000513673.1:n.*379-9_*379-8del
ENST00000698337.1:n.392_393del
ENST00000698338.1:n.816_817del
ENST00000698339.1:c.*38_*39del	ENSP00000513670.1:n.*38_*39del
ENST00000698340.1:c.552-224_552-223del	ENSP00000513671.1:n.552-224_552-223del
ENST00000162749.7:c.552-9_552-8del MANE Select	ENSP00000162749.2:n.552-9_552-8del
ENST00000162749.6:c.552-9_552-8del	ENSP00000162749.2:n.552-9_552-8del
ENST00000534885.5:c.*29-9_*29-8del	ENSP00000441803.1:n.*29-9_*29-8del
ENST00000535038.1:n.213_214del
ENST00000536717.5:n.447_448del
ENST00000537842.5:n.156-9_156-8del
ENST00000539372.5:c.552-9_552-8del	ENSP00000442059.1:n.552-9_552-8del
ENST00000540022.5:c.423-9_423-8del	ENSP00000438343.1:n.423-9_423-8del
ENST00000543359.5:n.38-224_38-223del
ENST00000543995.5:c.*139-9_*139-8del	ENSP00000442405.1:n.*139-9_*139-8del
NM_001065.3:c.552-9_552-8del , LRG_193t1:c.552-9_552-8del	NP_001056.1:n.552-9_552-8del
NM_001346091.1:c.228-9_228-8del	NP_001333020.1:n.228-9_228-8del
NM_001346092.1:c.93-9_93-8del	NP_001333021.1:n.93-9_93-8del
NR_144351.1:n.855-224_855-223del
NM_001065.4:c.552-9_552-8del MANE Select	NP_001056.1:n.552-9_552-8del
NM_001346091.2:c.228-9_228-8del	NP_001333020.1:n.228-9_228-8del
NM_001346092.2:c.93-9_93-8del	NP_001333021.1:n.93-9_93-8del
NR_144351.2:n.814-224_814-223del