Canonical Allele Identifier: CA6405429

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330665A>G , CM000674.2:g.6330665A>G	GRCh38
NC_000012.11:g.6439831A>G , CM000674.1:g.6439831A>G	GRCh37
NC_000012.10:g.6310092A>G	NCBI36
NG_007506.1:g.16431T>C , LRG_193:g.16431T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1773T>C
ENST00000437813.8:c.*133T>C	ENSP00000513672.1:n.*133T>C
ENST00000440083.7:c.891T>C	ENSP00000413224.3:p.Leu297=
ENST00000535038.2:n.854T>C
ENST00000535958.2:c.*499T>C	ENSP00000513673.1:n.*499T>C
ENST00000698337.1:n.662T>C
ENST00000698338.1:n.1086T>C
ENST00000698339.1:c.*167T>C	ENSP00000513670.1:n.*167T>C
ENST00000698340.1:c.598T>C	ENSP00000513671.1:p.Phe200Leu
ENST00000162749.7:c.672T>C MANE Select	ENSP00000162749.2:p.Leu224=
ENST00000162749.6:c.672T>C	ENSP00000162749.2:p.Leu224=
ENST00000534885.5:c.*149T>C	ENSP00000441803.1:n.*149T>C
ENST00000535038.1:n.483T>C
ENST00000536717.5:n.576T>C
ENST00000537842.5:n.276T>C
ENST00000539372.5:c.672T>C	ENSP00000442059.1:p.Leu224=
ENST00000540022.5:c.543T>C	ENSP00000438343.1:p.Leu181=
ENST00000543359.5:n.84T>C
ENST00000543995.5:c.*259T>C	ENSP00000442405.1:n.*259T>C
NM_001065.3:c.672T>C , LRG_193t1:c.672T>C	NP_001056.1:p.Leu224=
NM_001346091.1:c.348T>C	NP_001333020.1:p.Leu116=
NM_001346092.1:c.213T>C	NP_001333021.1:p.Leu71=
NR_144351.1:n.901T>C
NM_001065.4:c.672T>C MANE Select	NP_001056.1:p.Leu224=
NM_001346091.2:c.348T>C	NP_001333020.1:p.Leu116=
NM_001346092.2:c.213T>C	NP_001333021.1:p.Leu71=
NR_144351.2:n.860T>C