Canonical Allele Identifier: CA478112481

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439840A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330674A>G , CM000674.2:g.6330674A>G	GRCh38
NC_000012.11:g.6439840A>G , CM000674.1:g.6439840A>G	GRCh37
NC_000012.10:g.6310101A>G	NCBI36
NG_007506.1:g.16422T>C , LRG_193:g.16422T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1764T>C
ENST00000437813.8:c.*124T>C	ENSP00000513672.1:n.*124T>C
ENST00000440083.7:c.882T>C	ENSP00000413224.3:p.Gly294=
ENST00000535038.2:n.845T>C
ENST00000535958.2:c.*490T>C	ENSP00000513673.1:n.*490T>C
ENST00000698337.1:n.653T>C
ENST00000698338.1:n.1077T>C
ENST00000698339.1:c.*158T>C	ENSP00000513670.1:n.*158T>C
ENST00000698340.1:c.589T>C	ENSP00000513671.1:p.Ser197Pro
ENST00000162749.7:c.663T>C MANE Select	ENSP00000162749.2:p.Gly221=
ENST00000162749.6:c.663T>C	ENSP00000162749.2:p.Gly221=
ENST00000534885.5:c.*140T>C	ENSP00000441803.1:n.*140T>C
ENST00000535038.1:n.474T>C
ENST00000536717.5:n.567T>C
ENST00000537842.5:n.267T>C
ENST00000539372.5:c.663T>C	ENSP00000442059.1:p.Gly221=
ENST00000540022.5:c.534T>C	ENSP00000438343.1:p.Gly178=
ENST00000543359.5:n.75T>C
ENST00000543995.5:c.*250T>C	ENSP00000442405.1:n.*250T>C
NM_001065.3:c.663T>C , LRG_193t1:c.663T>C	NP_001056.1:p.Gly221=
NM_001346091.1:c.339T>C	NP_001333020.1:p.Gly113=
NM_001346092.1:c.204T>C	NP_001333021.1:p.Gly68=
NR_144351.1:n.892T>C
NM_001065.4:c.663T>C MANE Select	NP_001056.1:p.Gly221=
NM_001346091.2:c.339T>C	NP_001333020.1:p.Gly113=
NM_001346092.2:c.204T>C	NP_001333021.1:p.Gly68=
NR_144351.2:n.851T>C