Canonical Allele Identifier: CA383547784

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439849A>C (hg19) ; chr12:g.6330683A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330683A>C , CM000674.2:g.6330683A>C	GRCh38
NC_000012.11:g.6439849A>C , CM000674.1:g.6439849A>C	GRCh37
NC_000012.10:g.6310110A>C	NCBI36
NG_007506.1:g.16413T>G , LRG_193:g.16413T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1755T>G
ENST00000437813.8:c.*115T>G	ENSP00000513672.1:n.*115T>G
ENST00000440083.7:c.873T>G	ENSP00000413224.3:p.Ile291Met
ENST00000535038.2:n.836T>G
ENST00000535958.2:c.*481T>G	ENSP00000513673.1:n.*481T>G
ENST00000698337.1:n.644T>G
ENST00000698338.1:n.1068T>G
ENST00000698339.1:c.*149T>G	ENSP00000513670.1:n.*149T>G
ENST00000698340.1:c.580T>G	ENSP00000513671.1:p.Phe194Val
ENST00000162749.7:c.654T>G MANE Select	ENSP00000162749.2:p.Ile218Met
ENST00000162749.6:c.654T>G	ENSP00000162749.2:p.Ile218Met
ENST00000534885.5:c.*131T>G	ENSP00000441803.1:n.*131T>G
ENST00000535038.1:n.465T>G
ENST00000536717.5:n.558T>G
ENST00000537842.5:n.258T>G
ENST00000539372.5:c.654T>G	ENSP00000442059.1:p.Ile218Met
ENST00000540022.5:c.525T>G	ENSP00000438343.1:p.Ile175Met
ENST00000543359.5:n.66T>G
ENST00000543995.5:c.*241T>G	ENSP00000442405.1:n.*241T>G
NM_001065.3:c.654T>G , LRG_193t1:c.654T>G	NP_001056.1:p.Ile218Met
NM_001346091.1:c.330T>G	NP_001333020.1:p.Ile110Met
NM_001346092.1:c.195T>G	NP_001333021.1:p.Ile65Met
NR_144351.1:n.883T>G
NM_001065.4:c.654T>G MANE Select	NP_001056.1:p.Ile218Met
NM_001346091.2:c.330T>G	NP_001333020.1:p.Ile110Met
NM_001346092.2:c.195T>G	NP_001333021.1:p.Ile65Met
NR_144351.2:n.842T>G