Canonical Allele Identifier: CA383548152

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440080G>C (hg19) ; chr12:g.6330914G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330914G>C , CM000674.2:g.6330914G>C	GRCh38
NC_000012.11:g.6440080G>C , CM000674.1:g.6440080G>C	GRCh37
NC_000012.10:g.6310341G>C	NCBI36
NG_007506.1:g.16182C>G , LRG_193:g.16182C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1665C>G
ENST00000437813.8:c.*25C>G	ENSP00000513672.1:n.*25C>G
ENST00000440083.7:c.783C>G	ENSP00000413224.3:p.Ser261Arg
ENST00000535038.2:n.746C>G
ENST00000535958.2:c.*391C>G	ENSP00000513673.1:n.*391C>G
ENST00000698337.1:n.413C>G
ENST00000698338.1:n.837C>G
ENST00000698339.1:c.*59C>G	ENSP00000513670.1:n.*59C>G
ENST00000698340.1:c.552-203C>G	ENSP00000513671.1:n.552-203C>G
ENST00000162749.7:c.564C>G MANE Select	ENSP00000162749.2:p.Ser188Arg
ENST00000162749.6:c.564C>G	ENSP00000162749.2:p.Ser188Arg
ENST00000534885.5:c.*41C>G	ENSP00000441803.1:n.*41C>G
ENST00000535038.1:n.234C>G
ENST00000536717.5:n.468C>G
ENST00000537842.5:n.168C>G
ENST00000539372.5:c.564C>G	ENSP00000442059.1:p.Ser188Arg
ENST00000540022.5:c.435C>G	ENSP00000438343.1:p.Ser145Arg
ENST00000543359.5:n.38-203C>G
ENST00000543995.5:c.*151C>G	ENSP00000442405.1:n.*151C>G
NM_001065.3:c.564C>G , LRG_193t1:c.564C>G	NP_001056.1:p.Ser188Arg
NM_001346091.1:c.240C>G	NP_001333020.1:p.Ser80Arg
NM_001346092.1:c.105C>G	NP_001333021.1:p.Ser35Arg
NR_144351.1:n.855-203C>G
NM_001065.4:c.564C>G MANE Select	NP_001056.1:p.Ser188Arg
NM_001346091.2:c.240C>G	NP_001333020.1:p.Ser80Arg
NM_001346092.2:c.105C>G	NP_001333021.1:p.Ser35Arg
NR_144351.2:n.814-203C>G