Canonical Allele Identifier: CA383547772

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439847A>C (hg19) ; chr12:g.6330681A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330681A>C , CM000674.2:g.6330681A>C	GRCh38
NC_000012.11:g.6439847A>C , CM000674.1:g.6439847A>C	GRCh37
NC_000012.10:g.6310108A>C	NCBI36
NG_007506.1:g.16415T>G , LRG_193:g.16415T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1757T>G
ENST00000437813.8:c.*117T>G	ENSP00000513672.1:n.*117T>G
ENST00000440083.7:c.875T>G	ENSP00000413224.3:p.Phe292Cys
ENST00000535038.2:n.838T>G
ENST00000535958.2:c.*483T>G	ENSP00000513673.1:n.*483T>G
ENST00000698337.1:n.646T>G
ENST00000698338.1:n.1070T>G
ENST00000698339.1:c.*151T>G	ENSP00000513670.1:n.*151T>G
ENST00000698340.1:c.582T>G	ENSP00000513671.1:p.Phe194Leu
ENST00000162749.7:c.656T>G MANE Select	ENSP00000162749.2:p.Phe219Cys
ENST00000162749.6:c.656T>G	ENSP00000162749.2:p.Phe219Cys
ENST00000534885.5:c.*133T>G	ENSP00000441803.1:n.*133T>G
ENST00000535038.1:n.467T>G
ENST00000536717.5:n.560T>G
ENST00000537842.5:n.260T>G
ENST00000539372.5:c.656T>G	ENSP00000442059.1:p.Phe219Cys
ENST00000540022.5:c.527T>G	ENSP00000438343.1:p.Phe176Cys
ENST00000543359.5:n.68T>G
ENST00000543995.5:c.*243T>G	ENSP00000442405.1:n.*243T>G
NM_001065.3:c.656T>G , LRG_193t1:c.656T>G	NP_001056.1:p.Phe219Cys
NM_001346091.1:c.332T>G	NP_001333020.1:p.Phe111Cys
NM_001346092.1:c.197T>G	NP_001333021.1:p.Phe66Cys
NR_144351.1:n.885T>G
NM_001065.4:c.656T>G MANE Select	NP_001056.1:p.Phe219Cys
NM_001346091.2:c.332T>G	NP_001333020.1:p.Phe111Cys
NM_001346092.2:c.197T>G	NP_001333021.1:p.Phe66Cys
NR_144351.2:n.844T>G