Canonical Allele Identifier: CA383548088

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440061A>G (hg19) ; chr12:g.6330895A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330895A>G , CM000674.2:g.6330895A>G	GRCh38
NC_000012.11:g.6440061A>G , CM000674.1:g.6440061A>G	GRCh37
NC_000012.10:g.6310322A>G	NCBI36
NG_007506.1:g.16201T>C , LRG_193:g.16201T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1684T>C
ENST00000437813.8:c.*44T>C	ENSP00000513672.1:n.*44T>C
ENST00000440083.7:c.802T>C	ENSP00000413224.3:p.Cys268Arg
ENST00000535038.2:n.765T>C
ENST00000535958.2:c.*410T>C	ENSP00000513673.1:n.*410T>C
ENST00000698337.1:n.432T>C
ENST00000698338.1:n.856T>C
ENST00000698339.1:c.*78T>C	ENSP00000513670.1:n.*78T>C
ENST00000698340.1:c.552-184T>C	ENSP00000513671.1:n.552-184T>C
ENST00000162749.7:c.583T>C MANE Select	ENSP00000162749.2:p.Cys195Arg
ENST00000162749.6:c.583T>C	ENSP00000162749.2:p.Cys195Arg
ENST00000534885.5:c.*60T>C	ENSP00000441803.1:n.*60T>C
ENST00000535038.1:n.253T>C
ENST00000536717.5:n.487T>C
ENST00000537842.5:n.187T>C
ENST00000539372.5:c.583T>C	ENSP00000442059.1:p.Cys195Arg
ENST00000540022.5:c.454T>C	ENSP00000438343.1:p.Cys152Arg
ENST00000543359.5:n.38-184T>C
ENST00000543995.5:c.*170T>C	ENSP00000442405.1:n.*170T>C
NM_001065.3:c.583T>C , LRG_193t1:c.583T>C	NP_001056.1:p.Cys195Arg
NM_001346091.1:c.259T>C	NP_001333020.1:p.Cys87Arg
NM_001346092.1:c.124T>C	NP_001333021.1:p.Cys42Arg
NR_144351.1:n.855-184T>C
NM_001065.4:c.583T>C MANE Select	NP_001056.1:p.Cys195Arg
NM_001346091.2:c.259T>C	NP_001333020.1:p.Cys87Arg
NM_001346092.2:c.124T>C	NP_001333021.1:p.Cys42Arg
NR_144351.2:n.814-184T>C