Canonical Allele Identifier: CA2617250991

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6330832-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330833del , CM000674.2:g.6330833del	GRCh38
NC_000012.11:g.6439999del , CM000674.1:g.6439999del	GRCh37
NC_000012.10:g.6310260del	NCBI36
NG_007506.1:g.16263del , LRG_193:g.16263del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+20del
ENST00000437813.8:c.*86+20del	ENSP00000513672.1:n.*86+20del
ENST00000440083.7:c.844+20del	ENSP00000413224.3:n.844+20del
ENST00000535038.2:n.807+20del
ENST00000535958.2:c.*452+20del	ENSP00000513673.1:n.*452+20del
ENST00000698337.1:n.494del
ENST00000698338.1:n.918del
ENST00000698339.1:c.*120+20del	ENSP00000513670.1:n.*120+20del
ENST00000698340.1:c.552-122del	ENSP00000513671.1:n.552-122del
ENST00000162749.7:c.625+20del MANE Select	ENSP00000162749.2:n.625+20del
ENST00000162749.6:c.625+20del	ENSP00000162749.2:n.625+20del
ENST00000534885.5:c.*102+20del	ENSP00000441803.1:n.*102+20del
ENST00000535038.1:n.315del
ENST00000536717.5:n.529+20del
ENST00000537842.5:n.229+20del
ENST00000539372.5:c.625+20del	ENSP00000442059.1:n.625+20del
ENST00000540022.5:c.496+20del	ENSP00000438343.1:n.496+20del
ENST00000543359.5:n.38-122del
ENST00000543995.5:c.*212+20del	ENSP00000442405.1:n.*212+20del
NM_001065.3:c.625+20del , LRG_193t1:c.625+20del	NP_001056.1:n.625+20del
NM_001346091.1:c.301+20del	NP_001333020.1:n.301+20del
NM_001346092.1:c.166+20del	NP_001333021.1:n.166+20del
NR_144351.1:n.855-122del
NM_001065.4:c.625+20del MANE Select	NP_001056.1:n.625+20del
NM_001346091.2:c.301+20del	NP_001333020.1:n.301+20del
NM_001346092.2:c.166+20del	NP_001333021.1:n.166+20del
NR_144351.2:n.814-122del