Canonical Allele Identifier: CA2617251160

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330930-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330935_6330937del , CM000674.2:g.6330935_6330937del	GRCh38
NC_000012.11:g.6440101_6440103del , CM000674.1:g.6440101_6440103del	GRCh37
NC_000012.10:g.6310362_6310364del	NCBI36
NG_007506.1:g.16163_16165del , LRG_193:g.16163_16165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1646_1648del
ENST00000437813.8:c.*13-7_*13-5del	ENSP00000513672.1:n.*13-7_*13-5del
ENST00000440083.7:c.771-7_771-5del	ENSP00000413224.3:n.771-7_771-5del
ENST00000535038.2:n.727_729del
ENST00000535958.2:c.*379-7_*379-5del	ENSP00000513673.1:n.*379-7_*379-5del
ENST00000698337.1:n.394_396del
ENST00000698338.1:n.818_820del
ENST00000698339.1:c.*40_*42del	ENSP00000513670.1:n.*40_*42del
ENST00000698340.1:c.552-222_552-220del	ENSP00000513671.1:n.552-222_552-220del
ENST00000162749.7:c.552-7_552-5del MANE Select	ENSP00000162749.2:n.552-7_552-5del
ENST00000162749.6:c.552-7_552-5del	ENSP00000162749.2:n.552-7_552-5del
ENST00000534885.5:c.*29-7_*29-5del	ENSP00000441803.1:n.*29-7_*29-5del
ENST00000535038.1:n.215_217del
ENST00000536717.5:n.449_451del
ENST00000537842.5:n.156-7_156-5del
ENST00000539372.5:c.552-7_552-5del	ENSP00000442059.1:n.552-7_552-5del
ENST00000540022.5:c.423-7_423-5del	ENSP00000438343.1:n.423-7_423-5del
ENST00000543359.5:n.38-222_38-220del
ENST00000543995.5:c.*139-7_*139-5del	ENSP00000442405.1:n.*139-7_*139-5del
NM_001065.3:c.552-7_552-5del , LRG_193t1:c.552-7_552-5del	NP_001056.1:n.552-7_552-5del
NM_001346091.1:c.228-7_228-5del	NP_001333020.1:n.228-7_228-5del
NM_001346092.1:c.93-7_93-5del	NP_001333021.1:n.93-7_93-5del
NR_144351.1:n.855-222_855-220del
NM_001065.4:c.552-7_552-5del MANE Select	NP_001056.1:n.552-7_552-5del
NM_001346091.2:c.228-7_228-5del	NP_001333020.1:n.228-7_228-5del
NM_001346092.2:c.93-7_93-5del	NP_001333021.1:n.93-7_93-5del
NR_144351.2:n.814-222_814-220del