Canonical Allele Identifier: CA2617248782

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6329677-A-ATCCCGCGCCCTCCGCCTCTCGTGGTCCCCTCTGGGAGCGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329686_6329726dup , CM000674.2:g.6329686_6329726dup	GRCh38
NC_000012.11:g.6438852_6438892dup , CM000674.1:g.6438852_6438892dup	GRCh37
NC_000012.10:g.6309113_6309153dup	NCBI36
NG_007506.1:g.17378_17418dup , LRG_193:g.17378_17418dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.2158+60_2159-56dup
ENST00000437813.8:c.*518+60_*519-56dup	ENSP00000513672.1:n.*518+60_*519-56dup
ENST00000440083.7:c.1276+60_1277-56dup	ENSP00000413224.3:n.1276+60_1277-56dup
ENST00000535958.2:c.*884+60_*885-56dup	ENSP00000513673.1:n.*884+60_*885-56dup
ENST00000698337.1:n.1018+60_1019-56dup
ENST00000698338.1:n.1671+60_1672-56dup
ENST00000698339.1:c.*552+60_*553-56dup	ENSP00000513670.1:n.*552+60_*553-56dup
ENST00000698340.1:c.*296+60_*297-56dup	ENSP00000513671.1:n.*296+60_*297-56dup
ENST00000162749.7:c.1057+60_1058-56dup MANE Select	ENSP00000162749.2:n.1057+60_1058-56dup
ENST00000162749.6:c.1057+60_1058-56dup	ENSP00000162749.2:n.1057+60_1058-56dup
ENST00000534885.5:c.*534+60_*535-56dup	ENSP00000441803.1:n.*534+60_*535-56dup
ENST00000536717.5:n.961+60_962-56dup
ENST00000540022.5:c.928+60_929-56dup	ENSP00000438343.1:n.928+60_929-56dup
ENST00000543359.5:n.469+60_470-56dup
ENST00000543995.5:c.*644+60_*645-56dup	ENSP00000442405.1:n.*644+60_*645-56dup
NM_001065.3:c.1057+60_1058-56dup , LRG_193t1:c.1057+60_1058-56dup	NP_001056.1:n.1057+60_1058-56dup
NM_001346091.1:c.733+60_734-56dup	NP_001333020.1:n.733+60_734-56dup
NM_001346092.1:c.598+60_599-56dup	NP_001333021.1:n.598+60_599-56dup
NR_144351.1:n.1286+60_1287-56dup
NM_001065.4:c.1057+60_1058-56dup MANE Select	NP_001056.1:n.1057+60_1058-56dup
NM_001346091.2:c.733+60_734-56dup	NP_001333020.1:n.733+60_734-56dup
NM_001346092.2:c.598+60_599-56dup	NP_001333021.1:n.598+60_599-56dup
NR_144351.2:n.1245+60_1246-56dup