Canonical Allele Identifier: CA383550469

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442936T>C (hg19) ; chr12:g.6333770T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333770T>C , CM000674.2:g.6333770T>C	GRCh38
NC_000012.11:g.6442936T>C , CM000674.1:g.6442936T>C	GRCh37
NC_000012.10:g.6313197T>C	NCBI36
NG_007506.1:g.13326A>G , LRG_193:g.13326A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.323A>G
ENST00000437813.8:c.289A>G	ENSP00000513672.1:p.Arg97Gly
ENST00000440083.7:c.289A>G	ENSP00000413224.3:p.Arg97Gly
ENST00000535958.2:c.*116A>G	ENSP00000513673.1:n.*116A>G
ENST00000698339.1:c.289A>G	ENSP00000513670.1:p.Arg97Gly
ENST00000698340.1:c.289A>G	ENSP00000513671.1:p.Arg97Gly
ENST00000162749.7:c.289A>G MANE Select	ENSP00000162749.2:p.Arg97Gly
ENST00000162749.6:c.289A>G	ENSP00000162749.2:p.Arg97Gly
ENST00000366159.8:c.289A>G	ENSP00000380389.3:p.Arg97Gly
ENST00000437813.7:n.250A>G
ENST00000440083.6:c.289A>G	ENSP00000413224.2:p.Arg97Gly
ENST00000534885.5:c.135A>G	ENSP00000441803.1:p.Ser45=
ENST00000535958.1:n.535A>G
ENST00000536194.1:c.262A>G	ENSP00000442919.1:p.Arg88Gly
ENST00000539372.5:c.289A>G	ENSP00000442059.1:p.Arg97Gly
ENST00000540022.5:c.194-254A>G	ENSP00000438343.1:n.194-254A>G
ENST00000543048.5:c.214+75A>G	ENSP00000439981.1:n.214+75A>G
ENST00000543995.5:c.194-319A>G	ENSP00000442405.1:n.194-319A>G
NM_001065.3:c.289A>G , LRG_193t1:c.289A>G	NP_001056.1:p.Arg97Gly
NM_001346091.1:c.-36A>G	NP_001333020.1:n.-36A>G
NM_001346092.1:c.-289A>G	NP_001333021.1:n.-289A>G
NR_144351.1:n.592A>G
NM_001065.4:c.289A>G MANE Select	NP_001056.1:p.Arg97Gly
NM_001346091.2:c.-36A>G	NP_001333020.1:n.-36A>G
NM_001346092.2:c.-289A>G	NP_001333021.1:n.-289A>G
NR_144351.2:n.551A>G