Canonical Allele Identifier: CA2014026010

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333326G= , CM000674.2:g.6333326G=	GRCh38
NC_000012.11:g.6442492G= , CM000674.1:g.6442492G=	GRCh37
NC_000012.10:g.6312753G=	NCBI36
NG_007506.1:g.13770C= , LRG_193:g.13770C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.506+41C=
ENST00000437813.8:c.472+41C=	ENSP00000513672.1:n.472+41C=
ENST00000440083.7:c.513C=	ENSP00000413224.3:p.Pro171=
ENST00000535958.2:c.*299+41C=	ENSP00000513673.1:n.*299+41C=
ENST00000698339.1:c.472+41C=	ENSP00000513670.1:n.472+41C=
ENST00000698340.1:c.472+41C=	ENSP00000513671.1:n.472+41C=
ENST00000162749.7:c.472+41C= MANE Select	ENSP00000162749.2:n.472+41C=
ENST00000162749.6:c.472+41C=	ENSP00000162749.2:n.472+41C=
ENST00000366159.8:c.472+41C=	ENSP00000380389.3:n.472+41C=
ENST00000437813.7:n.433+41C=
ENST00000440083.6:c.513C=	ENSP00000413224.2:p.Pro171=
ENST00000534885.5:c.318+41C=	ENSP00000441803.1:n.318+41C=
ENST00000537842.5:n.76+41C=
ENST00000539372.5:c.472+41C=	ENSP00000442059.1:n.472+41C=
ENST00000540022.5:c.343+41C=	ENSP00000438343.1:n.343+41C=
ENST00000543048.5:c.*83+41C=	ENSP00000439981.1:n.*83+41C=
ENST00000543995.5:c.*59+41C=	ENSP00000442405.1:n.*59+41C=
NM_001065.3:c.472+41C= , LRG_193t1:c.472+41C=	NP_001056.1:n.472+41C=
NM_001346091.1:c.148+41C=	NP_001333020.1:n.148+41C=
NM_001346092.1:c.-106+41C=	NP_001333021.1:n.-106+41C=
NR_144351.1:n.775+41C=
NM_001065.4:c.472+41C= MANE Select	NP_001056.1:n.472+41C=
NM_001346091.2:c.148+41C=	NP_001333020.1:n.148+41C=
NM_001346092.2:c.-106+41C=	NP_001333021.1:n.-106+41C=
NR_144351.2:n.734+41C=