Canonical Allele Identifier: CA478113087

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442263T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333097T>G , CM000674.2:g.6333097T>G	GRCh38
NC_000012.11:g.6442263T>G , CM000674.1:g.6442263T>G	GRCh37
NC_000012.10:g.6312524T>G	NCBI36
NG_007506.1:g.13999A>C , LRG_193:g.13999A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.557A>C
ENST00000437813.8:c.523A>C	ENSP00000513672.1:p.Arg175=
ENST00000440083.7:c.742A>C	ENSP00000413224.3:p.Arg248=
ENST00000535958.2:c.*350A>C	ENSP00000513673.1:n.*350A>C
ENST00000698339.1:c.523A>C	ENSP00000513670.1:p.Arg175=
ENST00000698340.1:c.523A>C	ENSP00000513671.1:p.Arg175=
ENST00000162749.7:c.523A>C MANE Select	ENSP00000162749.2:p.Arg175=
ENST00000162749.6:c.523A>C	ENSP00000162749.2:p.Arg175=
ENST00000366159.8:c.523A>C	ENSP00000380389.3:p.Arg175=
ENST00000437813.7:n.484A>C
ENST00000440083.6:c.742A>C	ENSP00000413224.2:p.Arg248=
ENST00000534885.5:c.369A>C	ENSP00000441803.1:p.Ter123Tyr
ENST00000537842.5:n.127A>C
ENST00000539372.5:c.523A>C	ENSP00000442059.1:p.Arg175=
ENST00000540022.5:c.394A>C	ENSP00000438343.1:p.Arg132=
ENST00000543048.5:c.*134A>C	ENSP00000439981.1:n.*134A>C
ENST00000543359.5:n.9A>C
ENST00000543995.5:c.*110A>C	ENSP00000442405.1:n.*110A>C
NM_001065.3:c.523A>C , LRG_193t1:c.523A>C	NP_001056.1:p.Arg175=
NM_001346091.1:c.199A>C	NP_001333020.1:p.Arg67=
NM_001346092.1:c.-55A>C	NP_001333021.1:n.-55A>C
NR_144351.1:n.826A>C
NM_001065.4:c.523A>C MANE Select	NP_001056.1:p.Arg175=
NM_001346091.2:c.199A>C	NP_001333020.1:p.Arg67=
NM_001346092.2:c.-55A>C	NP_001333021.1:n.-55A>C
NR_144351.2:n.785A>C