Canonical Allele Identifier: CA2014025873

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333104G= , CM000674.2:g.6333104G=	GRCh38
NC_000012.11:g.6442270G= , CM000674.1:g.6442270G=	GRCh37
NC_000012.10:g.6312531G=	NCBI36
NG_007506.1:g.13992C= , LRG_193:g.13992C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.550C=
ENST00000437813.8:c.516C=	ENSP00000513672.1:p.Phe172=
ENST00000440083.7:c.735C=	ENSP00000413224.3:p.Phe245=
ENST00000535958.2:c.*343C=	ENSP00000513673.1:n.*343C=
ENST00000698339.1:c.516C=	ENSP00000513670.1:p.Phe172=
ENST00000698340.1:c.516C=	ENSP00000513671.1:p.Phe172=
ENST00000162749.7:c.516C= MANE Select	ENSP00000162749.2:p.Phe172=
ENST00000162749.6:c.516C=	ENSP00000162749.2:p.Phe172=
ENST00000366159.8:c.516C=	ENSP00000380389.3:p.Phe172=
ENST00000437813.7:n.477C=
ENST00000440083.6:c.735C=	ENSP00000413224.2:p.Phe245=
ENST00000534885.5:c.362C=	ENSP00000441803.1:p.Ser121=
ENST00000537842.5:n.120C=
ENST00000539372.5:c.516C=	ENSP00000442059.1:p.Phe172=
ENST00000540022.5:c.387C=	ENSP00000438343.1:p.Phe129=
ENST00000543048.5:c.*127C=	ENSP00000439981.1:n.*127C=
ENST00000543359.5:n.2C=
ENST00000543995.5:c.*103C=	ENSP00000442405.1:n.*103C=
NM_001065.3:c.516C= , LRG_193t1:c.516C=	NP_001056.1:p.Phe172=
NM_001346091.1:c.192C=	NP_001333020.1:p.Phe64=
NM_001346092.1:c.-62C=	NP_001333021.1:n.-62C=
NR_144351.1:n.819C=
NM_001065.4:c.516C= MANE Select	NP_001056.1:p.Phe172=
NM_001346091.2:c.192C=	NP_001333020.1:p.Phe64=
NM_001346092.2:c.-62C=	NP_001333021.1:n.-62C=
NR_144351.2:n.778C=