Canonical Allele Identifier: CA383547936

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6440019C>T (hg19) ; chr12:g.6330853C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330853C>T , CM000674.2:g.6330853C>T	GRCh38
NC_000012.11:g.6440019C>T , CM000674.1:g.6440019C>T	GRCh37
NC_000012.10:g.6310280C>T	NCBI36
NG_007506.1:g.16243G>A , LRG_193:g.16243G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1726G>A
ENST00000437813.8:c.*86G>A	ENSP00000513672.1:n.*86G>A
ENST00000440083.7:c.844G>A	ENSP00000413224.3:p.Gly282Ser
ENST00000535038.2:n.807G>A
ENST00000535958.2:c.*452G>A	ENSP00000513673.1:n.*452G>A
ENST00000698337.1:n.474G>A
ENST00000698338.1:n.898G>A
ENST00000698339.1:c.*120G>A	ENSP00000513670.1:n.*120G>A
ENST00000698340.1:c.552-142G>A	ENSP00000513671.1:n.552-142G>A
ENST00000162749.7:c.625G>A MANE Select	ENSP00000162749.2:p.Gly209Ser
ENST00000162749.6:c.625G>A	ENSP00000162749.2:p.Gly209Ser
ENST00000534885.5:c.*102G>A	ENSP00000441803.1:n.*102G>A
ENST00000535038.1:n.295G>A
ENST00000536717.5:n.529G>A
ENST00000537842.5:n.229G>A
ENST00000539372.5:c.625G>A	ENSP00000442059.1:p.Gly209Ser
ENST00000540022.5:c.496G>A	ENSP00000438343.1:p.Gly166Ser
ENST00000543359.5:n.38-142G>A
ENST00000543995.5:c.*212G>A	ENSP00000442405.1:n.*212G>A
NM_001065.3:c.625G>A , LRG_193t1:c.625G>A	NP_001056.1:p.Gly209Ser
NM_001346091.1:c.301G>A	NP_001333020.1:p.Gly101Ser
NM_001346092.1:c.166G>A	NP_001333021.1:p.Gly56Ser
NR_144351.1:n.855-142G>A
NM_001065.4:c.625G>A MANE Select	NP_001056.1:p.Gly209Ser
NM_001346091.2:c.301G>A	NP_001333020.1:p.Gly101Ser
NM_001346092.2:c.166G>A	NP_001333021.1:p.Gly56Ser
NR_144351.2:n.814-142G>A