Canonical Allele Identifier: CA2014025852

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333072C= , CM000674.2:g.6333072C=	GRCh38
NC_000012.11:g.6442238C= , CM000674.1:g.6442238C=	GRCh37
NC_000012.10:g.6312499C=	NCBI36
NG_007506.1:g.14024G= , LRG_193:g.14024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.582G=
ENST00000437813.8:c.548G=	ENSP00000513672.1:p.Ser183=
ENST00000440083.7:c.767G=	ENSP00000413224.3:p.Ser256=
ENST00000535958.2:c.*375G=	ENSP00000513673.1:n.*375G=
ENST00000698339.1:c.548G=	ENSP00000513670.1:p.Ser183=
ENST00000698340.1:c.548G=	ENSP00000513671.1:p.Ser183=
ENST00000162749.7:c.548G= MANE Select	ENSP00000162749.2:p.Ser183=
ENST00000162749.6:c.548G=	ENSP00000162749.2:p.Ser183=
ENST00000366159.8:c.548G=	ENSP00000380389.3:p.Ser183=
ENST00000437813.7:n.509G=
ENST00000534885.5:c.*25G=	ENSP00000441803.1:n.*25G=
ENST00000537842.5:n.152G=
ENST00000539372.5:c.548G=	ENSP00000442059.1:p.Ser183=
ENST00000540022.5:c.419G=	ENSP00000438343.1:p.Ser140=
ENST00000543048.5:c.*159G=	ENSP00000439981.1:n.*159G=
ENST00000543359.5:n.34G=
ENST00000543995.5:c.*135G=	ENSP00000442405.1:n.*135G=
NM_001065.3:c.548G= , LRG_193t1:c.548G=	NP_001056.1:p.Ser183=
NM_001346091.1:c.224G=	NP_001333020.1:p.Ser75=
NM_001346092.1:c.-30G=	NP_001333021.1:n.-30G=
NR_144351.1:n.851G=
NM_001065.4:c.548G= MANE Select	NP_001056.1:p.Ser183=
NM_001346091.2:c.224G=	NP_001333020.1:p.Ser75=
NM_001346092.2:c.-30G=	NP_001333021.1:n.-30G=
NR_144351.2:n.810G=