Canonical Allele Identifier: CA383548031

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440046C>T (hg19) ; chr12:g.6330880C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330880C>T , CM000674.2:g.6330880C>T	GRCh38
NC_000012.11:g.6440046C>T , CM000674.1:g.6440046C>T	GRCh37
NC_000012.10:g.6310307C>T	NCBI36
NG_007506.1:g.16216G>A , LRG_193:g.16216G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1699G>A
ENST00000437813.8:c.*59G>A	ENSP00000513672.1:n.*59G>A
ENST00000440083.7:c.817G>A	ENSP00000413224.3:p.Glu273Lys
ENST00000535038.2:n.780G>A
ENST00000535958.2:c.*425G>A	ENSP00000513673.1:n.*425G>A
ENST00000698337.1:n.447G>A
ENST00000698338.1:n.871G>A
ENST00000698339.1:c.*93G>A	ENSP00000513670.1:n.*93G>A
ENST00000698340.1:c.552-169G>A	ENSP00000513671.1:n.552-169G>A
ENST00000162749.7:c.598G>A MANE Select	ENSP00000162749.2:p.Glu200Lys
ENST00000162749.6:c.598G>A	ENSP00000162749.2:p.Glu200Lys
ENST00000534885.5:c.*75G>A	ENSP00000441803.1:n.*75G>A
ENST00000535038.1:n.268G>A
ENST00000536717.5:n.502G>A
ENST00000537842.5:n.202G>A
ENST00000539372.5:c.598G>A	ENSP00000442059.1:p.Glu200Lys
ENST00000540022.5:c.469G>A	ENSP00000438343.1:p.Glu157Lys
ENST00000543359.5:n.38-169G>A
ENST00000543995.5:c.*185G>A	ENSP00000442405.1:n.*185G>A
NM_001065.3:c.598G>A , LRG_193t1:c.598G>A	NP_001056.1:p.Glu200Lys
NM_001346091.1:c.274G>A	NP_001333020.1:p.Glu92Lys
NM_001346092.1:c.139G>A	NP_001333021.1:p.Glu47Lys
NR_144351.1:n.855-169G>A
NM_001065.4:c.598G>A MANE Select	NP_001056.1:p.Glu200Lys
NM_001346091.2:c.274G>A	NP_001333020.1:p.Glu92Lys
NM_001346092.2:c.139G>A	NP_001333021.1:p.Glu47Lys
NR_144351.2:n.814-169G>A