Canonical Allele Identifier: CA2014026055

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333406T= , CM000674.2:g.6333406T=	GRCh38
NC_000012.11:g.6442572T= , CM000674.1:g.6442572T=	GRCh37
NC_000012.10:g.6312833T=	NCBI36
NG_007506.1:g.13690A= , LRG_193:g.13690A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.467A=
ENST00000437813.8:c.433A=	ENSP00000513672.1:p.Asn145=
ENST00000440083.7:c.433A=	ENSP00000413224.3:p.Asn145=
ENST00000535958.2:c.*260A=	ENSP00000513673.1:n.*260A=
ENST00000698339.1:c.433A=	ENSP00000513670.1:p.Asn145=
ENST00000698340.1:c.433A=	ENSP00000513671.1:p.Asn145=
ENST00000162749.7:c.433A= MANE Select	ENSP00000162749.2:p.Asn145=
ENST00000162749.6:c.433A=	ENSP00000162749.2:p.Asn145=
ENST00000366159.8:c.433A=	ENSP00000380389.3:p.Asn145=
ENST00000437813.7:n.394A=
ENST00000440083.6:c.433A=	ENSP00000413224.2:p.Asn145=
ENST00000534885.5:c.279A=	ENSP00000441803.1:p.Ser93=
ENST00000537842.5:n.37A=
ENST00000539372.5:c.433A=	ENSP00000442059.1:p.Asn145=
ENST00000540022.5:c.304A=	ENSP00000438343.1:p.Asn102=
ENST00000543048.5:c.*44A=	ENSP00000439981.1:n.*44A=
ENST00000543995.5:c.*20A=	ENSP00000442405.1:n.*20A=
NM_001065.3:c.433A= , LRG_193t1:c.433A=	NP_001056.1:p.Asn145=
NM_001346091.1:c.109A=	NP_001333020.1:p.Asn37=
NM_001346092.1:c.-145A=	NP_001333021.1:n.-145A=
NR_144351.1:n.736A=
NM_001065.4:c.433A= MANE Select	NP_001056.1:p.Asn145=
NM_001346091.2:c.109A=	NP_001333020.1:p.Asn37=
NM_001346092.2:c.-145A=	NP_001333021.1:n.-145A=
NR_144351.2:n.695A=