Canonical Allele Identifier: CA478113086

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6442261T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333095T>C , CM000674.2:g.6333095T>C	GRCh38
NC_000012.11:g.6442261T>C , CM000674.1:g.6442261T>C	GRCh37
NC_000012.10:g.6312522T>C	NCBI36
NG_007506.1:g.14001A>G , LRG_193:g.14001A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.559A>G
ENST00000437813.8:c.525A>G	ENSP00000513672.1:p.Arg175=
ENST00000440083.7:c.744A>G	ENSP00000413224.3:p.Arg248=
ENST00000535958.2:c.*352A>G	ENSP00000513673.1:n.*352A>G
ENST00000698339.1:c.525A>G	ENSP00000513670.1:p.Arg175=
ENST00000698340.1:c.525A>G	ENSP00000513671.1:p.Arg175=
ENST00000162749.7:c.525A>G MANE Select	ENSP00000162749.2:p.Arg175=
ENST00000162749.6:c.525A>G	ENSP00000162749.2:p.Arg175=
ENST00000366159.8:c.525A>G	ENSP00000380389.3:p.Arg175=
ENST00000437813.7:n.486A>G
ENST00000440083.6:c.744A>G	ENSP00000413224.2:p.Arg248=
ENST00000534885.5:c.*2A>G	ENSP00000441803.1:n.*2A>G
ENST00000537842.5:n.129A>G
ENST00000539372.5:c.525A>G	ENSP00000442059.1:p.Arg175=
ENST00000540022.5:c.396A>G	ENSP00000438343.1:p.Arg132=
ENST00000543048.5:c.*136A>G	ENSP00000439981.1:n.*136A>G
ENST00000543359.5:n.11A>G
ENST00000543995.5:c.*112A>G	ENSP00000442405.1:n.*112A>G
NM_001065.3:c.525A>G , LRG_193t1:c.525A>G	NP_001056.1:p.Arg175=
NM_001346091.1:c.201A>G	NP_001333020.1:p.Arg67=
NM_001346092.1:c.-53A>G	NP_001333021.1:n.-53A>G
NR_144351.1:n.828A>G
NM_001065.4:c.525A>G MANE Select	NP_001056.1:p.Arg175=
NM_001346091.2:c.201A>G	NP_001333020.1:p.Arg67=
NM_001346092.2:c.-53A>G	NP_001333021.1:n.-53A>G
NR_144351.2:n.787A>G