Canonical Allele Identifier: CA2014026257

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333823G= , CM000674.2:g.6333823G=	GRCh38
NC_000012.11:g.6442989G= , CM000674.1:g.6442989G=	GRCh37
NC_000012.10:g.6313250G=	NCBI36
NG_007506.1:g.13273C= , LRG_193:g.13273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.270C=
ENST00000437813.8:c.236C=	ENSP00000513672.1:p.Thr79=
ENST00000440083.7:c.236C=	ENSP00000413224.3:p.Thr79=
ENST00000535958.2:c.*63C=	ENSP00000513673.1:n.*63C=
ENST00000698339.1:c.236C=	ENSP00000513670.1:p.Thr79=
ENST00000698340.1:c.236C=	ENSP00000513671.1:p.Thr79=
ENST00000162749.7:c.236C= MANE Select	ENSP00000162749.2:p.Thr79=
ENST00000162749.6:c.236C=	ENSP00000162749.2:p.Thr79=
ENST00000366159.8:c.236C=	ENSP00000380389.3:p.Thr79=
ENST00000437813.7:n.197C=
ENST00000440083.6:c.236C=	ENSP00000413224.2:p.Thr79=
ENST00000534885.5:c.82C=	ENSP00000441803.1:p.Arg28=
ENST00000535958.1:n.482C=
ENST00000536194.1:c.209C=	ENSP00000442919.1:p.Thr70=
ENST00000539372.5:c.236C=	ENSP00000442059.1:p.Thr79=
ENST00000540022.5:c.193+268C=	ENSP00000438343.1:n.193+268C=
ENST00000543048.5:c.214+22C=	ENSP00000439981.1:n.214+22C=
ENST00000543995.5:c.193+268C=	ENSP00000442405.1:n.193+268C=
NM_001065.3:c.236C= , LRG_193t1:c.236C=	NP_001056.1:p.Thr79=
NM_001346091.1:c.-89C=	NP_001333020.1:n.-89C=
NM_001346092.1:c.-342C=	NP_001333021.1:n.-342C=
NR_144351.1:n.539C=
NM_001065.4:c.236C= MANE Select	NP_001056.1:p.Thr79=
NM_001346091.2:c.-89C=	NP_001333020.1:n.-89C=
NM_001346092.2:c.-342C=	NP_001333021.1:n.-342C=
NR_144351.2:n.498C=