Canonical Allele Identifier: CA2014025911

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333138T= , CM000674.2:g.6333138T=	GRCh38
NC_000012.11:g.6442304T= , CM000674.1:g.6442304T=	GRCh37
NC_000012.10:g.6312565T=	NCBI36
NG_007506.1:g.13958A= , LRG_193:g.13958A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.516A=
ENST00000437813.8:c.482A=	ENSP00000513672.1:p.Lys161=
ENST00000440083.7:c.701A=	ENSP00000413224.3:p.Lys234=
ENST00000535958.2:c.*309A=	ENSP00000513673.1:n.*309A=
ENST00000698339.1:c.482A=	ENSP00000513670.1:p.Lys161=
ENST00000698340.1:c.482A=	ENSP00000513671.1:p.Lys161=
ENST00000162749.7:c.482A= MANE Select	ENSP00000162749.2:p.Lys161=
ENST00000162749.6:c.482A=	ENSP00000162749.2:p.Lys161=
ENST00000366159.8:c.482A=	ENSP00000380389.3:p.Lys161=
ENST00000437813.7:n.443A=
ENST00000440083.6:c.701A=	ENSP00000413224.2:p.Lys234=
ENST00000534885.5:c.328A=	ENSP00000441803.1:p.Asn110=
ENST00000537842.5:n.86A=
ENST00000539372.5:c.482A=	ENSP00000442059.1:p.Lys161=
ENST00000540022.5:c.353A=	ENSP00000438343.1:p.Lys118=
ENST00000543048.5:c.*93A=	ENSP00000439981.1:n.*93A=
ENST00000543995.5:c.*69A=	ENSP00000442405.1:n.*69A=
NM_001065.3:c.482A= , LRG_193t1:c.482A=	NP_001056.1:p.Lys161=
NM_001346091.1:c.158A=	NP_001333020.1:p.Lys53=
NM_001346092.1:c.-96A=	NP_001333021.1:n.-96A=
NR_144351.1:n.785A=
NM_001065.4:c.482A= MANE Select	NP_001056.1:p.Lys161=
NM_001346091.2:c.158A=	NP_001333020.1:p.Lys53=
NM_001346092.2:c.-96A=	NP_001333021.1:n.-96A=
NR_144351.2:n.744A=