Canonical Allele Identifier: CA232327354

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs201393951
• MyVariant Identifiers: chr12:g.6439841C>G (hg19) ; chr12:g.6330675C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330675C>G , CM000674.2:g.6330675C>G	GRCh38
NC_000012.11:g.6439841C>G , CM000674.1:g.6439841C>G	GRCh37
NC_000012.10:g.6310102C>G	NCBI36
NG_007506.1:g.16421G>C , LRG_193:g.16421G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1763G>C
ENST00000437813.8:c.*123G>C	ENSP00000513672.1:n.*123G>C
ENST00000440083.7:c.881G>C	ENSP00000413224.3:p.Gly294Ala
ENST00000535038.2:n.844G>C
ENST00000535958.2:c.*489G>C	ENSP00000513673.1:n.*489G>C
ENST00000698337.1:n.652G>C
ENST00000698338.1:n.1076G>C
ENST00000698339.1:c.*157G>C	ENSP00000513670.1:n.*157G>C
ENST00000698340.1:c.588G>C	ENSP00000513671.1:p.Trp196Cys
ENST00000162749.7:c.662G>C MANE Select	ENSP00000162749.2:p.Gly221Ala
ENST00000162749.6:c.662G>C	ENSP00000162749.2:p.Gly221Ala
ENST00000534885.5:c.*139G>C	ENSP00000441803.1:n.*139G>C
ENST00000535038.1:n.473G>C
ENST00000536717.5:n.566G>C
ENST00000537842.5:n.266G>C
ENST00000539372.5:c.662G>C	ENSP00000442059.1:p.Gly221Ala
ENST00000540022.5:c.533G>C	ENSP00000438343.1:p.Gly178Ala
ENST00000543359.5:n.74G>C
ENST00000543995.5:c.*249G>C	ENSP00000442405.1:n.*249G>C
NM_001065.3:c.662G>C , LRG_193t1:c.662G>C	NP_001056.1:p.Gly221Ala
NM_001346091.1:c.338G>C	NP_001333020.1:p.Gly113Ala
NM_001346092.1:c.203G>C	NP_001333021.1:p.Gly68Ala
NR_144351.1:n.891G>C
NM_001065.4:c.662G>C MANE Select	NP_001056.1:p.Gly221Ala
NM_001346091.2:c.338G>C	NP_001333020.1:p.Gly113Ala
NM_001346092.2:c.203G>C	NP_001333021.1:p.Gly68Ala
NR_144351.2:n.850G>C