Canonical Allele Identifier: CA2014024018

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330672A= , CM000674.2:g.6330672A=	GRCh38
NC_000012.11:g.6439838A= , CM000674.1:g.6439838A=	GRCh37
NC_000012.10:g.6310099A=	NCBI36
NG_007506.1:g.16424T= , LRG_193:g.16424T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1766T=
ENST00000437813.8:c.*126T=	ENSP00000513672.1:n.*126T=
ENST00000440083.7:c.884T=	ENSP00000413224.3:p.Leu295=
ENST00000535038.2:n.847T=
ENST00000535958.2:c.*492T=	ENSP00000513673.1:n.*492T=
ENST00000698337.1:n.655T=
ENST00000698338.1:n.1079T=
ENST00000698339.1:c.*160T=	ENSP00000513670.1:n.*160T=
ENST00000698340.1:c.591T=	ENSP00000513671.1:p.Ser197=
ENST00000162749.7:c.665T= MANE Select	ENSP00000162749.2:p.Leu222=
ENST00000162749.6:c.665T=	ENSP00000162749.2:p.Leu222=
ENST00000534885.5:c.*142T=	ENSP00000441803.1:n.*142T=
ENST00000535038.1:n.476T=
ENST00000536717.5:n.569T=
ENST00000537842.5:n.269T=
ENST00000539372.5:c.665T=	ENSP00000442059.1:p.Leu222=
ENST00000540022.5:c.536T=	ENSP00000438343.1:p.Leu179=
ENST00000543359.5:n.77T=
ENST00000543995.5:c.*252T=	ENSP00000442405.1:n.*252T=
NM_001065.3:c.665T= , LRG_193t1:c.665T=	NP_001056.1:p.Leu222=
NM_001346091.1:c.341T=	NP_001333020.1:p.Leu114=
NM_001346092.1:c.206T=	NP_001333021.1:p.Leu69=
NR_144351.1:n.894T=
NM_001065.4:c.665T= MANE Select	NP_001056.1:p.Leu222=
NM_001346091.2:c.341T=	NP_001333020.1:p.Leu114=
NM_001346092.2:c.206T=	NP_001333021.1:p.Leu69=
NR_144351.2:n.853T=