Canonical Allele Identifier: CA383548160

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440082T>G (hg19) ; chr12:g.6330916T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330916T>G , CM000674.2:g.6330916T>G	GRCh38
NC_000012.11:g.6440082T>G , CM000674.1:g.6440082T>G	GRCh37
NC_000012.10:g.6310343T>G	NCBI36
NG_007506.1:g.16180A>C , LRG_193:g.16180A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1663A>C
ENST00000437813.8:c.*23A>C	ENSP00000513672.1:n.*23A>C
ENST00000440083.7:c.781A>C	ENSP00000413224.3:p.Ser261Arg
ENST00000535038.2:n.744A>C
ENST00000535958.2:c.*389A>C	ENSP00000513673.1:n.*389A>C
ENST00000698337.1:n.411A>C
ENST00000698338.1:n.835A>C
ENST00000698339.1:c.*57A>C	ENSP00000513670.1:n.*57A>C
ENST00000698340.1:c.552-205A>C	ENSP00000513671.1:n.552-205A>C
ENST00000162749.7:c.562A>C MANE Select	ENSP00000162749.2:p.Ser188Arg
ENST00000162749.6:c.562A>C	ENSP00000162749.2:p.Ser188Arg
ENST00000534885.5:c.*39A>C	ENSP00000441803.1:n.*39A>C
ENST00000535038.1:n.232A>C
ENST00000536717.5:n.466A>C
ENST00000537842.5:n.166A>C
ENST00000539372.5:c.562A>C	ENSP00000442059.1:p.Ser188Arg
ENST00000540022.5:c.433A>C	ENSP00000438343.1:p.Ser145Arg
ENST00000543359.5:n.38-205A>C
ENST00000543995.5:c.*149A>C	ENSP00000442405.1:n.*149A>C
NM_001065.3:c.562A>C , LRG_193t1:c.562A>C	NP_001056.1:p.Ser188Arg
NM_001346091.1:c.238A>C	NP_001333020.1:p.Ser80Arg
NM_001346092.1:c.103A>C	NP_001333021.1:p.Ser35Arg
NR_144351.1:n.855-205A>C
NM_001065.4:c.562A>C MANE Select	NP_001056.1:p.Ser188Arg
NM_001346091.2:c.238A>C	NP_001333020.1:p.Ser80Arg
NM_001346092.2:c.103A>C	NP_001333021.1:p.Ser35Arg
NR_144351.2:n.814-205A>C