Canonical Allele Identifier: CA2014026087

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333478G= , CM000674.2:g.6333478G=	GRCh38
NC_000012.11:g.6442644G= , CM000674.1:g.6442644G=	GRCh37
NC_000012.10:g.6312905G=	NCBI36
NG_007506.1:g.13618C= , LRG_193:g.13618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.395C=
ENST00000437813.8:c.361C=	ENSP00000513672.1:p.Arg121=
ENST00000440083.7:c.361C=	ENSP00000413224.3:p.Arg121=
ENST00000535958.2:c.*188C=	ENSP00000513673.1:n.*188C=
ENST00000698339.1:c.361C=	ENSP00000513670.1:p.Arg121=
ENST00000698340.1:c.361C=	ENSP00000513671.1:p.Arg121=
ENST00000162749.7:c.361C= MANE Select	ENSP00000162749.2:p.Arg121=
ENST00000162749.6:c.361C=	ENSP00000162749.2:p.Arg121=
ENST00000366159.8:c.361C=	ENSP00000380389.3:p.Arg121=
ENST00000437813.7:n.322C=
ENST00000440083.6:c.361C=	ENSP00000413224.2:p.Arg121=
ENST00000534885.5:c.207C=	ENSP00000441803.1:p.Thr69=
ENST00000536194.1:c.334C=	ENSP00000442919.1:p.Arg112=
ENST00000539372.5:c.361C=	ENSP00000442059.1:p.Arg121=
ENST00000540022.5:c.232C=	ENSP00000438343.1:p.Arg78=
ENST00000543048.5:c.215-27C=	ENSP00000439981.1:n.215-27C=
ENST00000543995.5:c.194-27C=	ENSP00000442405.1:n.194-27C=
NM_001065.3:c.361C= , LRG_193t1:c.361C=	NP_001056.1:p.Arg121=
NM_001346091.1:c.37C=	NP_001333020.1:p.Arg13=
NM_001346092.1:c.-217C=	NP_001333021.1:n.-217C=
NR_144351.1:n.664C=
NM_001065.4:c.361C= MANE Select	NP_001056.1:p.Arg121=
NM_001346091.2:c.37C=	NP_001333020.1:p.Arg13=
NM_001346092.2:c.-217C=	NP_001333021.1:n.-217C=
NR_144351.2:n.623C=