Canonical Allele Identifier: CA2014026235

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333779T= , CM000674.2:g.6333779T=	GRCh38
NC_000012.11:g.6442945T= , CM000674.1:g.6442945T=	GRCh37
NC_000012.10:g.6313206T=	NCBI36
NG_007506.1:g.13317A= , LRG_193:g.13317A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.314A=
ENST00000437813.8:c.280A=	ENSP00000513672.1:p.Asn94=
ENST00000440083.7:c.280A=	ENSP00000413224.3:p.Asn94=
ENST00000535958.2:c.*107A=	ENSP00000513673.1:n.*107A=
ENST00000698339.1:c.280A=	ENSP00000513670.1:p.Asn94=
ENST00000698340.1:c.280A=	ENSP00000513671.1:p.Asn94=
ENST00000162749.7:c.280A= MANE Select	ENSP00000162749.2:p.Asn94=
ENST00000162749.6:c.280A=	ENSP00000162749.2:p.Asn94=
ENST00000366159.8:c.280A=	ENSP00000380389.3:p.Asn94=
ENST00000437813.7:n.241A=
ENST00000440083.6:c.280A=	ENSP00000413224.2:p.Asn94=
ENST00000534885.5:c.126A=	ENSP00000441803.1:p.Lys42=
ENST00000535958.1:n.526A=
ENST00000536194.1:c.253A=	ENSP00000442919.1:p.Asn85=
ENST00000539372.5:c.280A=	ENSP00000442059.1:p.Asn94=
ENST00000540022.5:c.194-263A=	ENSP00000438343.1:n.194-263A=
ENST00000543048.5:c.214+66A=	ENSP00000439981.1:n.214+66A=
ENST00000543995.5:c.193+312A=	ENSP00000442405.1:n.193+312A=
NM_001065.3:c.280A= , LRG_193t1:c.280A=	NP_001056.1:p.Asn94=
NM_001346091.1:c.-45A=	NP_001333020.1:n.-45A=
NM_001346092.1:c.-298A=	NP_001333021.1:n.-298A=
NR_144351.1:n.583A=
NM_001065.4:c.280A= MANE Select	NP_001056.1:p.Asn94=
NM_001346091.2:c.-45A=	NP_001333020.1:n.-45A=
NM_001346092.2:c.-298A=	NP_001333021.1:n.-298A=
NR_144351.2:n.542A=