Canonical Allele Identifier: CA2014026226

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333764A= , CM000674.2:g.6333764A=	GRCh38
NC_000012.11:g.6442930A= , CM000674.1:g.6442930A=	GRCh37
NC_000012.10:g.6313191A=	NCBI36
NG_007506.1:g.13332T= , LRG_193:g.13332T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.329T=
ENST00000437813.8:c.295T=	ENSP00000513672.1:p.Cys99=
ENST00000440083.7:c.295T=	ENSP00000413224.3:p.Cys99=
ENST00000535958.2:c.*122T=	ENSP00000513673.1:n.*122T=
ENST00000698339.1:c.295T=	ENSP00000513670.1:p.Cys99=
ENST00000698340.1:c.295T=	ENSP00000513671.1:p.Cys99=
ENST00000162749.7:c.295T= MANE Select	ENSP00000162749.2:p.Cys99=
ENST00000162749.6:c.295T=	ENSP00000162749.2:p.Cys99=
ENST00000366159.8:c.295T=	ENSP00000380389.3:p.Cys99=
ENST00000437813.7:n.256T=
ENST00000440083.6:c.295T=	ENSP00000413224.2:p.Cys99=
ENST00000534885.5:c.141T=	ENSP00000441803.1:p.Thr47=
ENST00000535958.1:n.541T=
ENST00000536194.1:c.268T=	ENSP00000442919.1:p.Cys90=
ENST00000539372.5:c.295T=	ENSP00000442059.1:p.Cys99=
ENST00000540022.5:c.194-248T=	ENSP00000438343.1:n.194-248T=
ENST00000543048.5:c.214+81T=	ENSP00000439981.1:n.214+81T=
ENST00000543995.5:c.194-313T=	ENSP00000442405.1:n.194-313T=
NM_001065.3:c.295T= , LRG_193t1:c.295T=	NP_001056.1:p.Cys99=
NM_001346091.1:c.-30T=	NP_001333020.1:n.-30T=
NM_001346092.1:c.-283T=	NP_001333021.1:n.-283T=
NR_144351.1:n.598T=
NM_001065.4:c.295T= MANE Select	NP_001056.1:p.Cys99=
NM_001346091.2:c.-30T=	NP_001333020.1:n.-30T=
NM_001346092.2:c.-283T=	NP_001333021.1:n.-283T=
NR_144351.2:n.557T=