Canonical Allele Identifier: CA383547749

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439842C>G (hg19) ; chr12:g.6330676C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330676C>G , CM000674.2:g.6330676C>G	GRCh38
NC_000012.11:g.6439842C>G , CM000674.1:g.6439842C>G	GRCh37
NC_000012.10:g.6310103C>G	NCBI36
NG_007506.1:g.16420G>C , LRG_193:g.16420G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1762G>C
ENST00000437813.8:c.*122G>C	ENSP00000513672.1:n.*122G>C
ENST00000440083.7:c.880G>C	ENSP00000413224.3:p.Gly294Arg
ENST00000535038.2:n.843G>C
ENST00000535958.2:c.*488G>C	ENSP00000513673.1:n.*488G>C
ENST00000698337.1:n.651G>C
ENST00000698338.1:n.1075G>C
ENST00000698339.1:c.*156G>C	ENSP00000513670.1:n.*156G>C
ENST00000698340.1:c.587G>C	ENSP00000513671.1:p.Trp196Ser
ENST00000162749.7:c.661G>C MANE Select	ENSP00000162749.2:p.Gly221Arg
ENST00000162749.6:c.661G>C	ENSP00000162749.2:p.Gly221Arg
ENST00000534885.5:c.*138G>C	ENSP00000441803.1:n.*138G>C
ENST00000535038.1:n.472G>C
ENST00000536717.5:n.565G>C
ENST00000537842.5:n.265G>C
ENST00000539372.5:c.661G>C	ENSP00000442059.1:p.Gly221Arg
ENST00000540022.5:c.532G>C	ENSP00000438343.1:p.Gly178Arg
ENST00000543359.5:n.73G>C
ENST00000543995.5:c.*248G>C	ENSP00000442405.1:n.*248G>C
NM_001065.3:c.661G>C , LRG_193t1:c.661G>C	NP_001056.1:p.Gly221Arg
NM_001346091.1:c.337G>C	NP_001333020.1:p.Gly113Arg
NM_001346092.1:c.202G>C	NP_001333021.1:p.Gly68Arg
NR_144351.1:n.890G>C
NM_001065.4:c.661G>C MANE Select	NP_001056.1:p.Gly221Arg
NM_001346091.2:c.337G>C	NP_001333020.1:p.Gly113Arg
NM_001346092.2:c.202G>C	NP_001333021.1:p.Gly68Arg
NR_144351.2:n.849G>C