Canonical Allele Identifier: CA2014026067

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333438T= , CM000674.2:g.6333438T=	GRCh38
NC_000012.11:g.6442604T= , CM000674.1:g.6442604T=	GRCh37
NC_000012.10:g.6312865T=	NCBI36
NG_007506.1:g.13658A= , LRG_193:g.13658A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.435A=
ENST00000437813.8:c.401A=	ENSP00000513672.1:p.His134=
ENST00000440083.7:c.401A=	ENSP00000413224.3:p.His134=
ENST00000535958.2:c.*228A=	ENSP00000513673.1:n.*228A=
ENST00000698339.1:c.401A=	ENSP00000513670.1:p.His134=
ENST00000698340.1:c.401A=	ENSP00000513671.1:p.His134=
ENST00000162749.7:c.401A= MANE Select	ENSP00000162749.2:p.His134=
ENST00000162749.6:c.401A=	ENSP00000162749.2:p.His134=
ENST00000366159.8:c.401A=	ENSP00000380389.3:p.His134=
ENST00000437813.7:n.362A=
ENST00000440083.6:c.401A=	ENSP00000413224.2:p.His134=
ENST00000534885.5:c.247A=	ENSP00000441803.1:p.Ile83=
ENST00000537842.5:n.5A=
ENST00000539372.5:c.401A=	ENSP00000442059.1:p.His134=
ENST00000540022.5:c.272A=	ENSP00000438343.1:p.His91=
ENST00000543048.5:c.*12A=	ENSP00000439981.1:n.*12A=
ENST00000543995.5:c.207A=	ENSP00000442405.1:p.Ala69=
NM_001065.3:c.401A= , LRG_193t1:c.401A=	NP_001056.1:p.His134=
NM_001346091.1:c.77A=	NP_001333020.1:p.His26=
NM_001346092.1:c.-177A=	NP_001333021.1:n.-177A=
NR_144351.1:n.704A=
NM_001065.4:c.401A= MANE Select	NP_001056.1:p.His134=
NM_001346091.2:c.77A=	NP_001333020.1:p.His26=
NM_001346092.2:c.-177A=	NP_001333021.1:n.-177A=
NR_144351.2:n.663A=