Canonical Allele Identifier: CA2014026252

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333816G= , CM000674.2:g.6333816G=	GRCh38
NC_000012.11:g.6442982G= , CM000674.1:g.6442982G=	GRCh37
NC_000012.10:g.6313243G=	NCBI36
NG_007506.1:g.13280C= , LRG_193:g.13280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.277C=
ENST00000437813.8:c.243C=	ENSP00000513672.1:p.Cys81=
ENST00000440083.7:c.243C=	ENSP00000413224.3:p.Cys81=
ENST00000535958.2:c.*70C=	ENSP00000513673.1:n.*70C=
ENST00000698339.1:c.243C=	ENSP00000513670.1:p.Cys81=
ENST00000698340.1:c.243C=	ENSP00000513671.1:p.Cys81=
ENST00000162749.7:c.243C= MANE Select	ENSP00000162749.2:p.Cys81=
ENST00000162749.6:c.243C=	ENSP00000162749.2:p.Cys81=
ENST00000366159.8:c.243C=	ENSP00000380389.3:p.Cys81=
ENST00000437813.7:n.204C=
ENST00000440083.6:c.243C=	ENSP00000413224.2:p.Cys81=
ENST00000534885.5:c.89C=	ENSP00000441803.1:p.Ala30=
ENST00000535958.1:n.489C=
ENST00000536194.1:c.216C=	ENSP00000442919.1:p.Cys72=
ENST00000539372.5:c.243C=	ENSP00000442059.1:p.Cys81=
ENST00000540022.5:c.193+275C=	ENSP00000438343.1:n.193+275C=
ENST00000543048.5:c.214+29C=	ENSP00000439981.1:n.214+29C=
ENST00000543995.5:c.193+275C=	ENSP00000442405.1:n.193+275C=
NM_001065.3:c.243C= , LRG_193t1:c.243C=	NP_001056.1:p.Cys81=
NM_001346091.1:c.-82C=	NP_001333020.1:n.-82C=
NM_001346092.1:c.-335C=	NP_001333021.1:n.-335C=
NR_144351.1:n.546C=
NM_001065.4:c.243C= MANE Select	NP_001056.1:p.Cys81=
NM_001346091.2:c.-82C=	NP_001333020.1:n.-82C=
NM_001346092.2:c.-335C=	NP_001333021.1:n.-335C=
NR_144351.2:n.505C=