Canonical Allele Identifier: CA2014026063

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333428A= , CM000674.2:g.6333428A=	GRCh38
NC_000012.11:g.6442594A= , CM000674.1:g.6442594A=	GRCh37
NC_000012.10:g.6312855A=	NCBI36
NG_007506.1:g.13668T= , LRG_193:g.13668T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.445T=
ENST00000437813.8:c.411T=	ENSP00000513672.1:p.Ser137=
ENST00000440083.7:c.411T=	ENSP00000413224.3:p.Ser137=
ENST00000535958.2:c.*238T=	ENSP00000513673.1:n.*238T=
ENST00000698339.1:c.411T=	ENSP00000513670.1:p.Ser137=
ENST00000698340.1:c.411T=	ENSP00000513671.1:p.Ser137=
ENST00000162749.7:c.411T= MANE Select	ENSP00000162749.2:p.Ser137=
ENST00000162749.6:c.411T=	ENSP00000162749.2:p.Ser137=
ENST00000366159.8:c.411T=	ENSP00000380389.3:p.Ser137=
ENST00000437813.7:n.372T=
ENST00000440083.6:c.411T=	ENSP00000413224.2:p.Ser137=
ENST00000534885.5:c.257T=	ENSP00000441803.1:p.Val86=
ENST00000537842.5:n.15T=
ENST00000539372.5:c.411T=	ENSP00000442059.1:p.Ser137=
ENST00000540022.5:c.282T=	ENSP00000438343.1:p.Ser94=
ENST00000543048.5:c.*22T=	ENSP00000439981.1:n.*22T=
ENST00000543995.5:c.217T=	ENSP00000442405.1:p.Ter73=
NM_001065.3:c.411T= , LRG_193t1:c.411T=	NP_001056.1:p.Ser137=
NM_001346091.1:c.87T=	NP_001333020.1:p.Ser29=
NM_001346092.1:c.-167T=	NP_001333021.1:n.-167T=
NR_144351.1:n.714T=
NM_001065.4:c.411T= MANE Select	NP_001056.1:p.Ser137=
NM_001346091.2:c.87T=	NP_001333020.1:p.Ser29=
NM_001346092.2:c.-167T=	NP_001333021.1:n.-167T=
NR_144351.2:n.673T=