Canonical Allele Identifier: CA603483608

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 1546740
• ClinVar RCV Id: RCV002175005
• dbSNP Id: rs1208890021
• gnomAD v2: 12-6440104-G-T
• gnomAD v3: 12-6330938-G-T
• gnomAD v4: 12-6330938-G-T
• MyVariant Identifiers: chr12:g.6440104G>T (hg19) ; chr12:g.6330938G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330938G>T , CM000674.2:g.6330938G>T	GRCh38
NC_000012.11:g.6440104G>T , CM000674.1:g.6440104G>T	GRCh37
NC_000012.10:g.6310365G>T	NCBI36
NG_007506.1:g.16158C>A , LRG_193:g.16158C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1641C>A
ENST00000437813.8:c.*13-12C>A	ENSP00000513672.1:n.*13-12C>A
ENST00000440083.7:c.771-12C>A	ENSP00000413224.3:n.771-12C>A
ENST00000535038.2:n.722C>A
ENST00000535958.2:c.*379-12C>A	ENSP00000513673.1:n.*379-12C>A
ENST00000698337.1:n.389C>A
ENST00000698338.1:n.813C>A
ENST00000698339.1:c.*35C>A	ENSP00000513670.1:n.*35C>A
ENST00000698340.1:c.552-227C>A	ENSP00000513671.1:n.552-227C>A
ENST00000162749.7:c.552-12C>A MANE Select	ENSP00000162749.2:n.552-12C>A
ENST00000162749.6:c.552-12C>A	ENSP00000162749.2:n.552-12C>A
ENST00000534885.5:c.*29-12C>A	ENSP00000441803.1:n.*29-12C>A
ENST00000535038.1:n.210C>A
ENST00000536717.5:n.444C>A
ENST00000537842.5:n.156-12C>A
ENST00000539372.5:c.552-12C>A	ENSP00000442059.1:n.552-12C>A
ENST00000540022.5:c.423-12C>A	ENSP00000438343.1:n.423-12C>A
ENST00000543359.5:n.38-227C>A
ENST00000543995.5:c.*139-12C>A	ENSP00000442405.1:n.*139-12C>A
NM_001065.3:c.552-12C>A , LRG_193t1:c.552-12C>A	NP_001056.1:n.552-12C>A
NM_001346091.1:c.228-12C>A	NP_001333020.1:n.228-12C>A
NM_001346092.1:c.93-12C>A	NP_001333021.1:n.93-12C>A
NR_144351.1:n.855-227C>A
NM_001065.4:c.552-12C>A MANE Select	NP_001056.1:n.552-12C>A
NM_001346091.2:c.228-12C>A	NP_001333020.1:n.228-12C>A
NM_001346092.2:c.93-12C>A	NP_001333021.1:n.93-12C>A
NR_144351.2:n.814-227C>A