Canonical Allele Identifier: CA2014025894

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333128G= , CM000674.2:g.6333128G=	GRCh38
NC_000012.11:g.6442294G= , CM000674.1:g.6442294G=	GRCh37
NC_000012.10:g.6312555G=	NCBI36
NG_007506.1:g.13968C= , LRG_193:g.13968C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.526C=
ENST00000437813.8:c.492C=	ENSP00000513672.1:p.Thr164=
ENST00000440083.7:c.711C=	ENSP00000413224.3:p.Thr237=
ENST00000535958.2:c.*319C=	ENSP00000513673.1:n.*319C=
ENST00000698339.1:c.492C=	ENSP00000513670.1:p.Thr164=
ENST00000698340.1:c.492C=	ENSP00000513671.1:p.Thr164=
ENST00000162749.7:c.492C= MANE Select	ENSP00000162749.2:p.Thr164=
ENST00000162749.6:c.492C=	ENSP00000162749.2:p.Thr164=
ENST00000366159.8:c.492C=	ENSP00000380389.3:p.Thr164=
ENST00000437813.7:n.453C=
ENST00000440083.6:c.711C=	ENSP00000413224.2:p.Thr237=
ENST00000534885.5:c.338C=	ENSP00000441803.1:p.Pro113=
ENST00000537842.5:n.96C=
ENST00000539372.5:c.492C=	ENSP00000442059.1:p.Thr164=
ENST00000540022.5:c.363C=	ENSP00000438343.1:p.Thr121=
ENST00000543048.5:c.*103C=	ENSP00000439981.1:n.*103C=
ENST00000543995.5:c.*79C=	ENSP00000442405.1:n.*79C=
NM_001065.3:c.492C= , LRG_193t1:c.492C=	NP_001056.1:p.Thr164=
NM_001346091.1:c.168C=	NP_001333020.1:p.Thr56=
NM_001346092.1:c.-86C=	NP_001333021.1:n.-86C=
NR_144351.1:n.795C=
NM_001065.4:c.492C= MANE Select	NP_001056.1:p.Thr164=
NM_001346091.2:c.168C=	NP_001333020.1:p.Thr56=
NM_001346092.2:c.-86C=	NP_001333021.1:n.-86C=
NR_144351.2:n.754C=