Canonical Allele Identifier: CA2014024009

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330659G= , CM000674.2:g.6330659G=	GRCh38
NC_000012.11:g.6439825G= , CM000674.1:g.6439825G=	GRCh37
NC_000012.10:g.6310086G=	NCBI36
NG_007506.1:g.16437C= , LRG_193:g.16437C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1779C=
ENST00000437813.8:c.*139C=	ENSP00000513672.1:n.*139C=
ENST00000440083.7:c.897C=	ENSP00000413224.3:p.Ser299=
ENST00000535038.2:n.860C=
ENST00000535958.2:c.*505C=	ENSP00000513673.1:n.*505C=
ENST00000698337.1:n.668C=
ENST00000698338.1:n.1092C=
ENST00000698339.1:c.*173C=	ENSP00000513670.1:n.*173C=
ENST00000698340.1:c.604C=	ENSP00000513671.1:p.Pro202=
ENST00000162749.7:c.678C= MANE Select	ENSP00000162749.2:p.Ser226=
ENST00000162749.6:c.678C=	ENSP00000162749.2:p.Ser226=
ENST00000534885.5:c.*155C=	ENSP00000441803.1:n.*155C=
ENST00000535038.1:n.489C=
ENST00000536717.5:n.582C=
ENST00000537842.5:n.282C=
ENST00000539372.5:c.678C=	ENSP00000442059.1:p.Ser226=
ENST00000540022.5:c.549C=	ENSP00000438343.1:p.Ser183=
ENST00000543359.5:n.90C=
ENST00000543995.5:c.*265C=	ENSP00000442405.1:n.*265C=
NM_001065.3:c.678C= , LRG_193t1:c.678C=	NP_001056.1:p.Ser226=
NM_001346091.1:c.354C=	NP_001333020.1:p.Ser118=
NM_001346092.1:c.219C=	NP_001333021.1:p.Ser73=
NR_144351.1:n.907C=
NM_001065.4:c.678C= MANE Select	NP_001056.1:p.Ser226=
NM_001346091.2:c.354C=	NP_001333020.1:p.Ser118=
NM_001346092.2:c.219C=	NP_001333021.1:p.Ser73=
NR_144351.2:n.866C=