Canonical Allele Identifier: CA2014026098

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333505C= , CM000674.2:g.6333505C=	GRCh38
NC_000012.11:g.6442671C= , CM000674.1:g.6442671C=	GRCh37
NC_000012.10:g.6312932C=	NCBI36
NG_007506.1:g.13591G= , LRG_193:g.13591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.368G=
ENST00000437813.8:c.334G=	ENSP00000513672.1:p.Val112=
ENST00000440083.7:c.334G=	ENSP00000413224.3:p.Val112=
ENST00000535958.2:c.*161G=	ENSP00000513673.1:n.*161G=
ENST00000698339.1:c.334G=	ENSP00000513670.1:p.Val112=
ENST00000698340.1:c.334G=	ENSP00000513671.1:p.Val112=
ENST00000162749.7:c.334G= MANE Select	ENSP00000162749.2:p.Val112=
ENST00000162749.6:c.334G=	ENSP00000162749.2:p.Val112=
ENST00000366159.8:c.334G=	ENSP00000380389.3:p.Val112=
ENST00000437813.7:n.295G=
ENST00000440083.6:c.334G=	ENSP00000413224.2:p.Val112=
ENST00000534885.5:c.180G=	ENSP00000441803.1:p.Arg60=
ENST00000536194.1:c.307G=	ENSP00000442919.1:p.Val103=
ENST00000539372.5:c.334G=	ENSP00000442059.1:p.Val112=
ENST00000540022.5:c.205G=	ENSP00000438343.1:p.Val69=
ENST00000543048.5:c.215-54G=	ENSP00000439981.1:n.215-54G=
ENST00000543995.5:c.194-54G=	ENSP00000442405.1:n.194-54G=
NM_001065.3:c.334G= , LRG_193t1:c.334G=	NP_001056.1:p.Val112=
NM_001346091.1:c.10G=	NP_001333020.1:p.Val4=
NM_001346092.1:c.-244G=	NP_001333021.1:n.-244G=
NR_144351.1:n.637G=
NM_001065.4:c.334G= MANE Select	NP_001056.1:p.Val112=
NM_001346091.2:c.10G=	NP_001333020.1:p.Val4=
NM_001346092.2:c.-244G=	NP_001333021.1:n.-244G=
NR_144351.2:n.596G=