Canonical Allele Identifier: CA383547573

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439796T>G (hg19) ; chr12:g.6330630T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330630T>G , CM000674.2:g.6330630T>G	GRCh38
NC_000012.11:g.6439796T>G , CM000674.1:g.6439796T>G	GRCh37
NC_000012.10:g.6310057T>G	NCBI36
NG_007506.1:g.16466A>C , LRG_193:g.16466A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1808A>C
ENST00000437813.8:c.*168A>C	ENSP00000513672.1:n.*168A>C
ENST00000440083.7:c.926A>C	ENSP00000413224.3:p.Tyr309Ser
ENST00000535038.2:n.889A>C
ENST00000535958.2:c.*534A>C	ENSP00000513673.1:n.*534A>C
ENST00000698337.1:n.697A>C
ENST00000698338.1:n.1121A>C
ENST00000698339.1:c.*202A>C	ENSP00000513670.1:n.*202A>C
ENST00000698340.1:c.633A>C	ENSP00000513671.1:p.Leu211=
ENST00000162749.7:c.707A>C MANE Select	ENSP00000162749.2:p.Tyr236Ser
ENST00000162749.6:c.707A>C	ENSP00000162749.2:p.Tyr236Ser
ENST00000534885.5:c.*184A>C	ENSP00000441803.1:n.*184A>C
ENST00000535038.1:n.518A>C
ENST00000536717.5:n.611A>C
ENST00000537842.5:n.311A>C
ENST00000539372.5:c.707A>C	ENSP00000442059.1:p.Tyr236Ser
ENST00000540022.5:c.578A>C	ENSP00000438343.1:p.Tyr193Ser
ENST00000543359.5:n.119A>C
ENST00000543995.5:c.*294A>C	ENSP00000442405.1:n.*294A>C
NM_001065.3:c.707A>C , LRG_193t1:c.707A>C	NP_001056.1:p.Tyr236Ser
NM_001346091.1:c.383A>C	NP_001333020.1:p.Tyr128Ser
NM_001346092.1:c.248A>C	NP_001333021.1:p.Tyr83Ser
NR_144351.1:n.936A>C
NM_001065.4:c.707A>C MANE Select	NP_001056.1:p.Tyr236Ser
NM_001346091.2:c.383A>C	NP_001333020.1:p.Tyr128Ser
NM_001346092.2:c.248A>C	NP_001333021.1:p.Tyr83Ser
NR_144351.2:n.895A>C