Canonical Allele Identifier: CA2014026227

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333767G= , CM000674.2:g.6333767G=	GRCh38
NC_000012.11:g.6442933G= , CM000674.1:g.6442933G=	GRCh37
NC_000012.10:g.6313194G=	NCBI36
NG_007506.1:g.13329C= , LRG_193:g.13329C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.326C=
ENST00000437813.8:c.292C=	ENSP00000513672.1:p.His98=
ENST00000440083.7:c.292C=	ENSP00000413224.3:p.His98=
ENST00000535958.2:c.*119C=	ENSP00000513673.1:n.*119C=
ENST00000698339.1:c.292C=	ENSP00000513670.1:p.His98=
ENST00000698340.1:c.292C=	ENSP00000513671.1:p.His98=
ENST00000162749.7:c.292C= MANE Select	ENSP00000162749.2:p.His98=
ENST00000162749.6:c.292C=	ENSP00000162749.2:p.His98=
ENST00000366159.8:c.292C=	ENSP00000380389.3:p.His98=
ENST00000437813.7:n.253C=
ENST00000440083.6:c.292C=	ENSP00000413224.2:p.His98=
ENST00000534885.5:c.138C=	ENSP00000441803.1:p.Asp46=
ENST00000535958.1:n.538C=
ENST00000536194.1:c.265C=	ENSP00000442919.1:p.His89=
ENST00000539372.5:c.292C=	ENSP00000442059.1:p.His98=
ENST00000540022.5:c.194-251C=	ENSP00000438343.1:n.194-251C=
ENST00000543048.5:c.214+78C=	ENSP00000439981.1:n.214+78C=
ENST00000543995.5:c.194-316C=	ENSP00000442405.1:n.194-316C=
NM_001065.3:c.292C= , LRG_193t1:c.292C=	NP_001056.1:p.His98=
NM_001346091.1:c.-33C=	NP_001333020.1:n.-33C=
NM_001346092.1:c.-286C=	NP_001333021.1:n.-286C=
NR_144351.1:n.595C=
NM_001065.4:c.292C= MANE Select	NP_001056.1:p.His98=
NM_001346091.2:c.-33C=	NP_001333020.1:n.-33C=
NM_001346092.2:c.-286C=	NP_001333021.1:n.-286C=
NR_144351.2:n.554C=