Canonical Allele Identifier: CA6405266

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6329597G>A , CM000674.2:g.6329597G>A	GRCh38
NC_000012.11:g.6438763G>A , CM000674.1:g.6438763G>A	GRCh37
NC_000012.10:g.6309024G>A	NCBI36
NG_007506.1:g.17499C>T , LRG_193:g.17499C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001065.4:c.1083C>T MANE Select	NP_001056.1:p.Ala361=
ENST00000162749.7:c.1083C>T MANE Select	ENSP00000162749.2:p.Ala361=
NM_001065.3:c.1083C>T , LRG_193t1:c.1083C>T	NP_001056.1:p.Ala361=
NM_001346091.1:c.759C>T	NP_001333020.1:p.Ala253=
NM_001346091.2:c.759C>T	NP_001333020.1:p.Ala253=
NM_001346092.1:c.624C>T	NP_001333021.1:p.Ala208=
NM_001346092.2:c.624C>T	NP_001333021.1:p.Ala208=
NR_144351.1:n.1312C>T
NR_144351.2:n.1271C>T
ENST00000162749.6:c.1083C>T	ENSP00000162749.2:p.Ala361=
ENST00000366159.9:n.2184C>T
ENST00000437813.8:c.*544C>T	ENSP00000513672.1:n.*544C>T
ENST00000440083.7:c.1302C>T	ENSP00000413224.3:p.Ala434=
ENST00000534885.5:c.*560C>T	ENSP00000441803.1:n.*560C>T
ENST00000535958.2:c.*910C>T	ENSP00000513673.1:n.*910C>T
ENST00000536717.5:n.987C>T
ENST00000540022.5:c.954C>T	ENSP00000438343.1:p.Ala318=
ENST00000543359.5:n.495C>T
ENST00000543995.5:c.*670C>T	ENSP00000442405.1:n.*670C>T
ENST00000698337.1:n.1044C>T
ENST00000698338.1:n.1697C>T
ENST00000698339.1:c.*578C>T	ENSP00000513670.1:n.*578C>T
ENST00000698340.1:c.*322C>T	ENSP00000513671.1:n.*322C>T