Canonical Allele Identifier: CA383548058

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440054G>T (hg19) ; chr12:g.6330888G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330888G>T , CM000674.2:g.6330888G>T	GRCh38
NC_000012.11:g.6440054G>T , CM000674.1:g.6440054G>T	GRCh37
NC_000012.10:g.6310315G>T	NCBI36
NG_007506.1:g.16208C>A , LRG_193:g.16208C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1691C>A
ENST00000437813.8:c.*51C>A	ENSP00000513672.1:n.*51C>A
ENST00000440083.7:c.809C>A	ENSP00000413224.3:p.Pro270His
ENST00000535038.2:n.772C>A
ENST00000535958.2:c.*417C>A	ENSP00000513673.1:n.*417C>A
ENST00000698337.1:n.439C>A
ENST00000698338.1:n.863C>A
ENST00000698339.1:c.*85C>A	ENSP00000513670.1:n.*85C>A
ENST00000698340.1:c.552-177C>A	ENSP00000513671.1:n.552-177C>A
ENST00000162749.7:c.590C>A MANE Select	ENSP00000162749.2:p.Pro197His
ENST00000162749.6:c.590C>A	ENSP00000162749.2:p.Pro197His
ENST00000534885.5:c.*67C>A	ENSP00000441803.1:n.*67C>A
ENST00000535038.1:n.260C>A
ENST00000536717.5:n.494C>A
ENST00000537842.5:n.194C>A
ENST00000539372.5:c.590C>A	ENSP00000442059.1:p.Pro197His
ENST00000540022.5:c.461C>A	ENSP00000438343.1:p.Pro154His
ENST00000543359.5:n.38-177C>A
ENST00000543995.5:c.*177C>A	ENSP00000442405.1:n.*177C>A
NM_001065.3:c.590C>A , LRG_193t1:c.590C>A	NP_001056.1:p.Pro197His
NM_001346091.1:c.266C>A	NP_001333020.1:p.Pro89His
NM_001346092.1:c.131C>A	NP_001333021.1:p.Pro44His
NR_144351.1:n.855-177C>A
NM_001065.4:c.590C>A MANE Select	NP_001056.1:p.Pro197His
NM_001346091.2:c.266C>A	NP_001333020.1:p.Pro89His
NM_001346092.2:c.131C>A	NP_001333021.1:p.Pro44His
NR_144351.2:n.814-177C>A