Canonical Allele Identifier: CA383549879

Gene: TNFRSF1A

Linked Data

• COSMIC: COSM942434
• MyVariant Identifiers: chr12:g.6442548T>C (hg19) ; chr12:g.6333382T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333382T>C , CM000674.2:g.6333382T>C	GRCh38
NC_000012.11:g.6442548T>C , CM000674.1:g.6442548T>C	GRCh37
NC_000012.10:g.6312809T>C	NCBI36
NG_007506.1:g.13714A>G , LRG_193:g.13714A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.491A>G
ENST00000437813.8:c.457A>G	ENSP00000513672.1:p.Thr153Ala
ENST00000440083.7:c.457A>G	ENSP00000413224.3:p.Thr153Ala
ENST00000535958.2:c.*284A>G	ENSP00000513673.1:n.*284A>G
ENST00000698339.1:c.457A>G	ENSP00000513670.1:p.Thr153Ala
ENST00000698340.1:c.457A>G	ENSP00000513671.1:p.Thr153Ala
ENST00000162749.7:c.457A>G MANE Select	ENSP00000162749.2:p.Thr153Ala
ENST00000162749.6:c.457A>G	ENSP00000162749.2:p.Thr153Ala
ENST00000366159.8:c.457A>G	ENSP00000380389.3:p.Thr153Ala
ENST00000437813.7:n.418A>G
ENST00000440083.6:c.457A>G	ENSP00000413224.2:p.Thr153Ala
ENST00000534885.5:c.303A>G	ENSP00000441803.1:p.Gly101=
ENST00000537842.5:n.61A>G
ENST00000539372.5:c.457A>G	ENSP00000442059.1:p.Thr153Ala
ENST00000540022.5:c.328A>G	ENSP00000438343.1:p.Thr110Ala
ENST00000543048.5:c.*68A>G	ENSP00000439981.1:n.*68A>G
ENST00000543995.5:c.*44A>G	ENSP00000442405.1:n.*44A>G
NM_001065.3:c.457A>G , LRG_193t1:c.457A>G	NP_001056.1:p.Thr153Ala
NM_001346091.1:c.133A>G	NP_001333020.1:p.Thr45Ala
NM_001346092.1:c.-121A>G	NP_001333021.1:n.-121A>G
NR_144351.1:n.760A>G
NM_001065.4:c.457A>G MANE Select	NP_001056.1:p.Thr153Ala
NM_001346091.2:c.133A>G	NP_001333020.1:p.Thr45Ala
NM_001346092.2:c.-121A>G	NP_001333021.1:n.-121A>G
NR_144351.2:n.719A>G