Canonical Allele Identifier: CA2014026238

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333790G= , CM000674.2:g.6333790G=	GRCh38
NC_000012.11:g.6442956G= , CM000674.1:g.6442956G=	GRCh37
NC_000012.10:g.6313217G=	NCBI36
NG_007506.1:g.13306C= , LRG_193:g.13306C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.303C=
ENST00000437813.8:c.269C=	ENSP00000513672.1:p.Thr90=
ENST00000440083.7:c.269C=	ENSP00000413224.3:p.Thr90=
ENST00000535958.2:c.*96C=	ENSP00000513673.1:n.*96C=
ENST00000698339.1:c.269C=	ENSP00000513670.1:p.Thr90=
ENST00000698340.1:c.269C=	ENSP00000513671.1:p.Thr90=
ENST00000162749.7:c.269C= MANE Select	ENSP00000162749.2:p.Thr90=
ENST00000162749.6:c.269C=	ENSP00000162749.2:p.Thr90=
ENST00000366159.8:c.269C=	ENSP00000380389.3:p.Thr90=
ENST00000437813.7:n.230C=
ENST00000440083.6:c.269C=	ENSP00000413224.2:p.Thr90=
ENST00000534885.5:c.115C=	ENSP00000441803.1:p.Pro39=
ENST00000535958.1:n.515C=
ENST00000536194.1:c.242C=	ENSP00000442919.1:p.Thr81=
ENST00000539372.5:c.269C=	ENSP00000442059.1:p.Thr90=
ENST00000540022.5:c.194-274C=	ENSP00000438343.1:n.194-274C=
ENST00000543048.5:c.214+55C=	ENSP00000439981.1:n.214+55C=
ENST00000543995.5:c.193+301C=	ENSP00000442405.1:n.193+301C=
NM_001065.3:c.269C= , LRG_193t1:c.269C=	NP_001056.1:p.Thr90=
NM_001346091.1:c.-56C=	NP_001333020.1:n.-56C=
NM_001346092.1:c.-309C=	NP_001333021.1:n.-309C=
NR_144351.1:n.572C=
NM_001065.4:c.269C= MANE Select	NP_001056.1:p.Thr90=
NM_001346091.2:c.-56C=	NP_001333020.1:n.-56C=
NM_001346092.2:c.-309C=	NP_001333021.1:n.-309C=
NR_144351.2:n.531C=