Canonical Allele Identifier: CA383547970

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440026C>G (hg19) ; chr12:g.6330860C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330860C>G , CM000674.2:g.6330860C>G	GRCh38
NC_000012.11:g.6440026C>G , CM000674.1:g.6440026C>G	GRCh37
NC_000012.10:g.6310287C>G	NCBI36
NG_007506.1:g.16236G>C , LRG_193:g.16236G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1719G>C
ENST00000437813.8:c.*79G>C	ENSP00000513672.1:n.*79G>C
ENST00000440083.7:c.837G>C	ENSP00000413224.3:p.Glu279Asp
ENST00000535038.2:n.800G>C
ENST00000535958.2:c.*445G>C	ENSP00000513673.1:n.*445G>C
ENST00000698337.1:n.467G>C
ENST00000698338.1:n.891G>C
ENST00000698339.1:c.*113G>C	ENSP00000513670.1:n.*113G>C
ENST00000698340.1:c.552-149G>C	ENSP00000513671.1:n.552-149G>C
ENST00000162749.7:c.618G>C MANE Select	ENSP00000162749.2:p.Glu206Asp
ENST00000162749.6:c.618G>C	ENSP00000162749.2:p.Glu206Asp
ENST00000534885.5:c.*95G>C	ENSP00000441803.1:n.*95G>C
ENST00000535038.1:n.288G>C
ENST00000536717.5:n.522G>C
ENST00000537842.5:n.222G>C
ENST00000539372.5:c.618G>C	ENSP00000442059.1:p.Glu206Asp
ENST00000540022.5:c.489G>C	ENSP00000438343.1:p.Glu163Asp
ENST00000543359.5:n.38-149G>C
ENST00000543995.5:c.*205G>C	ENSP00000442405.1:n.*205G>C
NM_001065.3:c.618G>C , LRG_193t1:c.618G>C	NP_001056.1:p.Glu206Asp
NM_001346091.1:c.294G>C	NP_001333020.1:p.Glu98Asp
NM_001346092.1:c.159G>C	NP_001333021.1:p.Glu53Asp
NR_144351.1:n.855-149G>C
NM_001065.4:c.618G>C MANE Select	NP_001056.1:p.Glu206Asp
NM_001346091.2:c.294G>C	NP_001333020.1:p.Glu98Asp
NM_001346092.2:c.159G>C	NP_001333021.1:p.Glu53Asp
NR_144351.2:n.814-149G>C