Canonical Allele Identifier: CA478112313

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439798G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330632G>A , CM000674.2:g.6330632G>A	GRCh38
NC_000012.11:g.6439798G>A , CM000674.1:g.6439798G>A	GRCh37
NC_000012.10:g.6310059G>A	NCBI36
NG_007506.1:g.16464C>T , LRG_193:g.16464C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1806C>T
ENST00000437813.8:c.*166C>T	ENSP00000513672.1:n.*166C>T
ENST00000440083.7:c.924C>T	ENSP00000413224.3:p.Arg308=
ENST00000535038.2:n.887C>T
ENST00000535958.2:c.*532C>T	ENSP00000513673.1:n.*532C>T
ENST00000698337.1:n.695C>T
ENST00000698338.1:n.1119C>T
ENST00000698339.1:c.*200C>T	ENSP00000513670.1:n.*200C>T
ENST00000698340.1:c.631C>T	ENSP00000513671.1:p.Leu211=
ENST00000162749.7:c.705C>T MANE Select	ENSP00000162749.2:p.Arg235=
ENST00000162749.6:c.705C>T	ENSP00000162749.2:p.Arg235=
ENST00000534885.5:c.*182C>T	ENSP00000441803.1:n.*182C>T
ENST00000535038.1:n.516C>T
ENST00000536717.5:n.609C>T
ENST00000537842.5:n.309C>T
ENST00000539372.5:c.705C>T	ENSP00000442059.1:p.Arg235=
ENST00000540022.5:c.576C>T	ENSP00000438343.1:p.Arg192=
ENST00000543359.5:n.117C>T
ENST00000543995.5:c.*292C>T	ENSP00000442405.1:n.*292C>T
NM_001065.3:c.705C>T , LRG_193t1:c.705C>T	NP_001056.1:p.Arg235=
NM_001346091.1:c.381C>T	NP_001333020.1:p.Arg127=
NM_001346092.1:c.246C>T	NP_001333021.1:p.Arg82=
NR_144351.1:n.934C>T
NM_001065.4:c.705C>T MANE Select	NP_001056.1:p.Arg235=
NM_001346091.2:c.381C>T	NP_001333020.1:p.Arg127=
NM_001346092.2:c.246C>T	NP_001333021.1:p.Arg82=
NR_144351.2:n.893C>T