Canonical Allele Identifier: CA2739271834

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 2840600
• ClinVar RCV Id: RCV003625673

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330835C>T , CM000674.2:g.6330835C>T	GRCh38
NC_000012.11:g.6440001C>T , CM000674.1:g.6440001C>T	GRCh37
NC_000012.10:g.6310262C>T	NCBI36
NG_007506.1:g.16261G>A , LRG_193:g.16261G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726+18G>A
ENST00000437813.8:c.*86+18G>A	ENSP00000513672.1:n.*86+18G>A
ENST00000440083.7:c.844+18G>A	ENSP00000413224.3:n.844+18G>A
ENST00000535038.2:n.807+18G>A
ENST00000535958.2:c.*452+18G>A	ENSP00000513673.1:n.*452+18G>A
ENST00000698337.1:n.492G>A
ENST00000698338.1:n.916G>A
ENST00000698339.1:c.*120+18G>A	ENSP00000513670.1:n.*120+18G>A
ENST00000698340.1:c.552-124G>A	ENSP00000513671.1:n.552-124G>A
ENST00000162749.7:c.625+18G>A MANE Select	ENSP00000162749.2:n.625+18G>A
ENST00000162749.6:c.625+18G>A	ENSP00000162749.2:n.625+18G>A
ENST00000534885.5:c.*102+18G>A	ENSP00000441803.1:n.*102+18G>A
ENST00000535038.1:n.313G>A
ENST00000536717.5:n.529+18G>A
ENST00000537842.5:n.229+18G>A
ENST00000539372.5:c.625+18G>A	ENSP00000442059.1:n.625+18G>A
ENST00000540022.5:c.496+18G>A	ENSP00000438343.1:n.496+18G>A
ENST00000543359.5:n.38-124G>A
ENST00000543995.5:c.*212+18G>A	ENSP00000442405.1:n.*212+18G>A
NM_001065.3:c.625+18G>A , LRG_193t1:c.625+18G>A	NP_001056.1:n.625+18G>A
NM_001346091.1:c.301+18G>A	NP_001333020.1:n.301+18G>A
NM_001346092.1:c.166+18G>A	NP_001333021.1:n.166+18G>A
NR_144351.1:n.855-124G>A
NM_001065.4:c.625+18G>A MANE Select	NP_001056.1:n.625+18G>A
NM_001346091.2:c.301+18G>A	NP_001333020.1:n.301+18G>A
NM_001346092.2:c.166+18G>A	NP_001333021.1:n.166+18G>A
NR_144351.2:n.814-124G>A