Canonical Allele Identifier: CA2014026090

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333489C= , CM000674.2:g.6333489C=	GRCh38
NC_000012.11:g.6442655C= , CM000674.1:g.6442655C=	GRCh37
NC_000012.10:g.6312916C=	NCBI36
NG_007506.1:g.13607G= , LRG_193:g.13607G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.384G=
ENST00000437813.8:c.350G=	ENSP00000513672.1:p.Cys117=
ENST00000440083.7:c.350G=	ENSP00000413224.3:p.Cys117=
ENST00000535958.2:c.*177G=	ENSP00000513673.1:n.*177G=
ENST00000698339.1:c.350G=	ENSP00000513670.1:p.Cys117=
ENST00000698340.1:c.350G=	ENSP00000513671.1:p.Cys117=
ENST00000162749.7:c.350G= MANE Select	ENSP00000162749.2:p.Cys117=
ENST00000162749.6:c.350G=	ENSP00000162749.2:p.Cys117=
ENST00000366159.8:c.350G=	ENSP00000380389.3:p.Cys117=
ENST00000437813.7:n.311G=
ENST00000440083.6:c.350G=	ENSP00000413224.2:p.Cys117=
ENST00000534885.5:c.196G=	ENSP00000441803.1:p.Ala66=
ENST00000536194.1:c.323G=	ENSP00000442919.1:p.Cys108=
ENST00000539372.5:c.350G=	ENSP00000442059.1:p.Cys117=
ENST00000540022.5:c.221G=	ENSP00000438343.1:p.Cys74=
ENST00000543048.5:c.215-38G=	ENSP00000439981.1:n.215-38G=
ENST00000543995.5:c.194-38G=	ENSP00000442405.1:n.194-38G=
NM_001065.3:c.350G= , LRG_193t1:c.350G=	NP_001056.1:p.Cys117=
NM_001346091.1:c.26G=	NP_001333020.1:p.Cys9=
NM_001346092.1:c.-228G=	NP_001333021.1:n.-228G=
NR_144351.1:n.653G=
NM_001065.4:c.350G= MANE Select	NP_001056.1:p.Cys117=
NM_001346091.2:c.26G=	NP_001333020.1:p.Cys9=
NM_001346092.2:c.-228G=	NP_001333021.1:n.-228G=
NR_144351.2:n.612G=