Canonical Allele Identifier: CA383548053

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440052G>C (hg19) ; chr12:g.6330886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330886G>C , CM000674.2:g.6330886G>C	GRCh38
NC_000012.11:g.6440052G>C , CM000674.1:g.6440052G>C	GRCh37
NC_000012.10:g.6310313G>C	NCBI36
NG_007506.1:g.16210C>G , LRG_193:g.16210C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1693C>G
ENST00000437813.8:c.*53C>G	ENSP00000513672.1:n.*53C>G
ENST00000440083.7:c.811C>G	ENSP00000413224.3:p.Gln271Glu
ENST00000535038.2:n.774C>G
ENST00000535958.2:c.*419C>G	ENSP00000513673.1:n.*419C>G
ENST00000698337.1:n.441C>G
ENST00000698338.1:n.865C>G
ENST00000698339.1:c.*87C>G	ENSP00000513670.1:n.*87C>G
ENST00000698340.1:c.552-175C>G	ENSP00000513671.1:n.552-175C>G
ENST00000162749.7:c.592C>G MANE Select	ENSP00000162749.2:p.Gln198Glu
ENST00000162749.6:c.592C>G	ENSP00000162749.2:p.Gln198Glu
ENST00000534885.5:c.*69C>G	ENSP00000441803.1:n.*69C>G
ENST00000535038.1:n.262C>G
ENST00000536717.5:n.496C>G
ENST00000537842.5:n.196C>G
ENST00000539372.5:c.592C>G	ENSP00000442059.1:p.Gln198Glu
ENST00000540022.5:c.463C>G	ENSP00000438343.1:p.Gln155Glu
ENST00000543359.5:n.38-175C>G
ENST00000543995.5:c.*179C>G	ENSP00000442405.1:n.*179C>G
NM_001065.3:c.592C>G , LRG_193t1:c.592C>G	NP_001056.1:p.Gln198Glu
NM_001346091.1:c.268C>G	NP_001333020.1:p.Gln90Glu
NM_001346092.1:c.133C>G	NP_001333021.1:p.Gln45Glu
NR_144351.1:n.855-175C>G
NM_001065.4:c.592C>G MANE Select	NP_001056.1:p.Gln198Glu
NM_001346091.2:c.268C>G	NP_001333020.1:p.Gln90Glu
NM_001346092.2:c.133C>G	NP_001333021.1:p.Gln45Glu
NR_144351.2:n.814-175C>G