Canonical Allele Identifier: CA2617248788

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6329683-CGCCCTCCGCCTCTCGTGGTCCCCTCTGGGAGCGCCTCCCGCGCTCCCCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329691_6329740del , CM000674.2:g.6329691_6329740del	GRCh38
NC_000012.11:g.6438857_6438906del , CM000674.1:g.6438857_6438906del	GRCh37
NC_000012.10:g.6309118_6309167del	NCBI36
NG_007506.1:g.17363_17412del , LRG_193:g.17363_17412del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2158+45_2159-62del
ENST00000437813.8:c.*518+45_*519-62del	ENSP00000513672.1:n.*518+45_*519-62del
ENST00000440083.7:c.1276+45_1277-62del	ENSP00000413224.3:n.1276+45_1277-62del
ENST00000535958.2:c.*884+45_*885-62del	ENSP00000513673.1:n.*884+45_*885-62del
ENST00000698337.1:n.1018+45_1019-62del
ENST00000698338.1:n.1671+45_1672-62del
ENST00000698339.1:c.*552+45_*553-62del	ENSP00000513670.1:n.*552+45_*553-62del
ENST00000698340.1:c.*296+45_*297-62del	ENSP00000513671.1:n.*296+45_*297-62del
ENST00000162749.7:c.1057+45_1058-62del MANE Select	ENSP00000162749.2:n.1057+45_1058-62del
ENST00000162749.6:c.1057+45_1058-62del	ENSP00000162749.2:n.1057+45_1058-62del
ENST00000534885.5:c.*534+45_*535-62del	ENSP00000441803.1:n.*534+45_*535-62del
ENST00000536717.5:n.961+45_962-62del
ENST00000540022.5:c.928+45_929-62del	ENSP00000438343.1:n.928+45_929-62del
ENST00000543359.5:n.469+45_470-62del
ENST00000543995.5:c.*644+45_*645-62del	ENSP00000442405.1:n.*644+45_*645-62del
NM_001065.3:c.1057+45_1058-62del , LRG_193t1:c.1057+45_1058-62del	NP_001056.1:n.1057+45_1058-62del
NM_001346091.1:c.733+45_734-62del	NP_001333020.1:n.733+45_734-62del
NM_001346092.1:c.598+45_599-62del	NP_001333021.1:n.598+45_599-62del
NR_144351.1:n.1286+45_1287-62del
NM_001065.4:c.1057+45_1058-62del MANE Select	NP_001056.1:n.1057+45_1058-62del
NM_001346091.2:c.733+45_734-62del	NP_001333020.1:n.733+45_734-62del
NM_001346092.2:c.598+45_599-62del	NP_001333021.1:n.598+45_599-62del
NR_144351.2:n.1245+45_1246-62del