Canonical Allele Identifier: CA478113094

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs2136821264
• MyVariant Identifiers: chr12:g.6442273A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333107A>C , CM000674.2:g.6333107A>C	GRCh38
NC_000012.11:g.6442273A>C , CM000674.1:g.6442273A>C	GRCh37
NC_000012.10:g.6312534A>C	NCBI36
NG_007506.1:g.13989T>G , LRG_193:g.13989T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.547T>G
ENST00000437813.8:c.513T>G	ENSP00000513672.1:p.Gly171=
ENST00000440083.7:c.732T>G	ENSP00000413224.3:p.Gly244=
ENST00000535958.2:c.*340T>G	ENSP00000513673.1:n.*340T>G
ENST00000698339.1:c.513T>G	ENSP00000513670.1:p.Gly171=
ENST00000698340.1:c.513T>G	ENSP00000513671.1:p.Gly171=
ENST00000162749.7:c.513T>G MANE Select	ENSP00000162749.2:p.Gly171=
ENST00000162749.6:c.513T>G	ENSP00000162749.2:p.Gly171=
ENST00000366159.8:c.513T>G	ENSP00000380389.3:p.Gly171=
ENST00000437813.7:n.474T>G
ENST00000440083.6:c.732T>G	ENSP00000413224.2:p.Gly244=
ENST00000534885.5:c.359T>G	ENSP00000441803.1:p.Val120Gly
ENST00000537842.5:n.117T>G
ENST00000539372.5:c.513T>G	ENSP00000442059.1:p.Gly171=
ENST00000540022.5:c.384T>G	ENSP00000438343.1:p.Gly128=
ENST00000543048.5:c.*124T>G	ENSP00000439981.1:n.*124T>G
ENST00000543995.5:c.*100T>G	ENSP00000442405.1:n.*100T>G
NM_001065.3:c.513T>G , LRG_193t1:c.513T>G	NP_001056.1:p.Gly171=
NM_001346091.1:c.189T>G	NP_001333020.1:p.Gly63=
NM_001346092.1:c.-65T>G	NP_001333021.1:n.-65T>G
NR_144351.1:n.816T>G
NM_001065.4:c.513T>G MANE Select	NP_001056.1:p.Gly171=
NM_001346091.2:c.189T>G	NP_001333020.1:p.Gly63=
NM_001346092.2:c.-65T>G	NP_001333021.1:n.-65T>G
NR_144351.2:n.775T>G