Canonical Allele Identifier: CA2014024290

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330926G= , CM000674.2:g.6330926G=	GRCh38
NC_000012.11:g.6440092G= , CM000674.1:g.6440092G=	GRCh37
NC_000012.10:g.6310353G=	NCBI36
NG_007506.1:g.16170C= , LRG_193:g.16170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1653C=
ENST00000437813.8:c.*13C=	ENSP00000513672.1:n.*13C=
ENST00000440083.7:c.771C=	ENSP00000413224.3:p.Asn257=
ENST00000535038.2:n.734C=
ENST00000535958.2:c.*379C=	ENSP00000513673.1:n.*379C=
ENST00000698337.1:n.401C=
ENST00000698338.1:n.825C=
ENST00000698339.1:c.*47C=	ENSP00000513670.1:n.*47C=
ENST00000698340.1:c.552-215C=	ENSP00000513671.1:n.552-215C=
ENST00000162749.7:c.552C= MANE Select	ENSP00000162749.2:p.Asn184=
ENST00000162749.6:c.552C=	ENSP00000162749.2:p.Asn184=
ENST00000534885.5:c.*29C=	ENSP00000441803.1:n.*29C=
ENST00000535038.1:n.222C=
ENST00000536717.5:n.456C=
ENST00000537842.5:n.156C=
ENST00000539372.5:c.552C=	ENSP00000442059.1:p.Asn184=
ENST00000540022.5:c.423C=	ENSP00000438343.1:p.Asn141=
ENST00000543359.5:n.38-215C=
ENST00000543995.5:c.*139C=	ENSP00000442405.1:n.*139C=
NM_001065.3:c.552C= , LRG_193t1:c.552C=	NP_001056.1:p.Asn184=
NM_001346091.1:c.228C=	NP_001333020.1:p.Asn76=
NM_001346092.1:c.93C=	NP_001333021.1:p.Ser31=
NR_144351.1:n.855-215C=
NM_001065.4:c.552C= MANE Select	NP_001056.1:p.Asn184=
NM_001346091.2:c.228C=	NP_001333020.1:p.Asn76=
NM_001346092.2:c.93C=	NP_001333021.1:p.Ser31=
NR_144351.2:n.814-215C=