Canonical Allele Identifier: CA478112375

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439813A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330647A>G , CM000674.2:g.6330647A>G	GRCh38
NC_000012.11:g.6439813A>G , CM000674.1:g.6439813A>G	GRCh37
NC_000012.10:g.6310074A>G	NCBI36
NG_007506.1:g.16449T>C , LRG_193:g.16449T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1791T>C
ENST00000437813.8:c.*151T>C	ENSP00000513672.1:n.*151T>C
ENST00000440083.7:c.909T>C	ENSP00000413224.3:p.Ile303=
ENST00000535038.2:n.872T>C
ENST00000535958.2:c.*517T>C	ENSP00000513673.1:n.*517T>C
ENST00000698337.1:n.680T>C
ENST00000698338.1:n.1104T>C
ENST00000698339.1:c.*185T>C	ENSP00000513670.1:n.*185T>C
ENST00000698340.1:c.616T>C	ENSP00000513671.1:p.Trp206Arg
ENST00000162749.7:c.690T>C MANE Select	ENSP00000162749.2:p.Ile230=
ENST00000162749.6:c.690T>C	ENSP00000162749.2:p.Ile230=
ENST00000534885.5:c.*167T>C	ENSP00000441803.1:n.*167T>C
ENST00000535038.1:n.501T>C
ENST00000536717.5:n.594T>C
ENST00000537842.5:n.294T>C
ENST00000539372.5:c.690T>C	ENSP00000442059.1:p.Ile230=
ENST00000540022.5:c.561T>C	ENSP00000438343.1:p.Ile187=
ENST00000543359.5:n.102T>C
ENST00000543995.5:c.*277T>C	ENSP00000442405.1:n.*277T>C
NM_001065.3:c.690T>C , LRG_193t1:c.690T>C	NP_001056.1:p.Ile230=
NM_001346091.1:c.366T>C	NP_001333020.1:p.Ile122=
NM_001346092.1:c.231T>C	NP_001333021.1:p.Ile77=
NR_144351.1:n.919T>C
NM_001065.4:c.690T>C MANE Select	NP_001056.1:p.Ile230=
NM_001346091.2:c.366T>C	NP_001333020.1:p.Ile122=
NM_001346092.2:c.231T>C	NP_001333021.1:p.Ile77=
NR_144351.2:n.878T>C