Canonical Allele Identifier: CA6405246

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329483C>A , CM000674.2:g.6329483C>A	GRCh38
NC_000012.11:g.6438649C>A , CM000674.1:g.6438649C>A	GRCh37
NC_000012.10:g.6308910C>A	NCBI36
NG_007506.1:g.17613G>T , LRG_193:g.17613G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.2298G>T
ENST00000437813.8:c.*658G>T	ENSP00000513672.1:n.*658G>T
ENST00000440083.7:c.1416G>T	ENSP00000413224.3:p.Ala472=
ENST00000535958.2:c.*1024G>T	ENSP00000513673.1:n.*1024G>T
ENST00000698337.1:n.1158G>T
ENST00000698338.1:n.1811G>T
ENST00000698339.1:c.*692G>T	ENSP00000513670.1:n.*692G>T
ENST00000698340.1:c.*436G>T	ENSP00000513671.1:n.*436G>T
ENST00000162749.7:c.1197G>T MANE Select	ENSP00000162749.2:p.Ala399=
ENST00000162749.6:c.1197G>T	ENSP00000162749.2:p.Ala399=
ENST00000534885.5:c.*674G>T	ENSP00000441803.1:n.*674G>T
ENST00000536717.5:n.1101G>T
ENST00000540022.5:c.1068G>T	ENSP00000438343.1:p.Ala356=
ENST00000543359.5:n.609G>T
ENST00000543995.5:c.*784G>T	ENSP00000442405.1:n.*784G>T
NM_001065.3:c.1197G>T , LRG_193t1:c.1197G>T	NP_001056.1:p.Ala399=
NM_001346091.1:c.873G>T	NP_001333020.1:p.Ala291=
NM_001346092.1:c.738G>T	NP_001333021.1:p.Ala246=
NR_144351.1:n.1426G>T
NM_001065.4:c.1197G>T MANE Select	NP_001056.1:p.Ala399=
NM_001346091.2:c.873G>T	NP_001333020.1:p.Ala291=
NM_001346092.2:c.738G>T	NP_001333021.1:p.Ala246=
NR_144351.2:n.1385G>T