Canonical Allele Identifier: CA383548182

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440087T>C (hg19) ; chr12:g.6330921T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330921T>C , CM000674.2:g.6330921T>C	GRCh38
NC_000012.11:g.6440087T>C , CM000674.1:g.6440087T>C	GRCh37
NC_000012.10:g.6310348T>C	NCBI36
NG_007506.1:g.16175A>G , LRG_193:g.16175A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1658A>G
ENST00000437813.8:c.*18A>G	ENSP00000513672.1:n.*18A>G
ENST00000440083.7:c.776A>G	ENSP00000413224.3:p.Lys259Arg
ENST00000535038.2:n.739A>G
ENST00000535958.2:c.*384A>G	ENSP00000513673.1:n.*384A>G
ENST00000698337.1:n.406A>G
ENST00000698338.1:n.830A>G
ENST00000698339.1:c.*52A>G	ENSP00000513670.1:n.*52A>G
ENST00000698340.1:c.552-210A>G	ENSP00000513671.1:n.552-210A>G
ENST00000162749.7:c.557A>G MANE Select	ENSP00000162749.2:p.Lys186Arg
ENST00000162749.6:c.557A>G	ENSP00000162749.2:p.Lys186Arg
ENST00000534885.5:c.*34A>G	ENSP00000441803.1:n.*34A>G
ENST00000535038.1:n.227A>G
ENST00000536717.5:n.461A>G
ENST00000537842.5:n.161A>G
ENST00000539372.5:c.557A>G	ENSP00000442059.1:p.Lys186Arg
ENST00000540022.5:c.428A>G	ENSP00000438343.1:p.Lys143Arg
ENST00000543359.5:n.38-210A>G
ENST00000543995.5:c.*144A>G	ENSP00000442405.1:n.*144A>G
NM_001065.3:c.557A>G , LRG_193t1:c.557A>G	NP_001056.1:p.Lys186Arg
NM_001346091.1:c.233A>G	NP_001333020.1:p.Lys78Arg
NM_001346092.1:c.98A>G	NP_001333021.1:p.Lys33Arg
NR_144351.1:n.855-210A>G
NM_001065.4:c.557A>G MANE Select	NP_001056.1:p.Lys186Arg
NM_001346091.2:c.233A>G	NP_001333020.1:p.Lys78Arg
NM_001346092.2:c.98A>G	NP_001333021.1:p.Lys33Arg
NR_144351.2:n.814-210A>G