Canonical Allele Identifier: CA383547589

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439801A>C (hg19) ; chr12:g.6330635A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330635A>C , CM000674.2:g.6330635A>C	GRCh38
NC_000012.11:g.6439801A>C , CM000674.1:g.6439801A>C	GRCh37
NC_000012.10:g.6310062A>C	NCBI36
NG_007506.1:g.16461T>G , LRG_193:g.16461T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1803T>G
ENST00000437813.8:c.*163T>G	ENSP00000513672.1:n.*163T>G
ENST00000440083.7:c.921T>G	ENSP00000413224.3:p.Tyr307Ter
ENST00000535038.2:n.884T>G
ENST00000535958.2:c.*529T>G	ENSP00000513673.1:n.*529T>G
ENST00000698337.1:n.692T>G
ENST00000698338.1:n.1116T>G
ENST00000698339.1:c.*197T>G	ENSP00000513670.1:n.*197T>G
ENST00000698340.1:c.628T>G	ENSP00000513671.1:p.Ser210Ala
ENST00000162749.7:c.702T>G MANE Select	ENSP00000162749.2:p.Tyr234Ter
ENST00000162749.6:c.702T>G	ENSP00000162749.2:p.Tyr234Ter
ENST00000534885.5:c.*179T>G	ENSP00000441803.1:n.*179T>G
ENST00000535038.1:n.513T>G
ENST00000536717.5:n.606T>G
ENST00000537842.5:n.306T>G
ENST00000539372.5:c.702T>G	ENSP00000442059.1:p.Tyr234Ter
ENST00000540022.5:c.573T>G	ENSP00000438343.1:p.Tyr191Ter
ENST00000543359.5:n.114T>G
ENST00000543995.5:c.*289T>G	ENSP00000442405.1:n.*289T>G
NM_001065.3:c.702T>G , LRG_193t1:c.702T>G	NP_001056.1:p.Tyr234Ter
NM_001346091.1:c.378T>G	NP_001333020.1:p.Tyr126Ter
NM_001346092.1:c.243T>G	NP_001333021.1:p.Tyr81Ter
NR_144351.1:n.931T>G
NM_001065.4:c.702T>G MANE Select	NP_001056.1:p.Tyr234Ter
NM_001346091.2:c.378T>G	NP_001333020.1:p.Tyr126Ter
NM_001346092.2:c.243T>G	NP_001333021.1:p.Tyr81Ter
NR_144351.2:n.890T>G