Canonical Allele Identifier: CA2014024252

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330904T= , CM000674.2:g.6330904T=	GRCh38
NC_000012.11:g.6440070T= , CM000674.1:g.6440070T=	GRCh37
NC_000012.10:g.6310331T=	NCBI36
NG_007506.1:g.16192A= , LRG_193:g.16192A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1675A=
ENST00000437813.8:c.*35A=	ENSP00000513672.1:n.*35A=
ENST00000440083.7:c.793A=	ENSP00000413224.3:p.Thr265=
ENST00000535038.2:n.756A=
ENST00000535958.2:c.*401A=	ENSP00000513673.1:n.*401A=
ENST00000698337.1:n.423A=
ENST00000698338.1:n.847A=
ENST00000698339.1:c.*69A=	ENSP00000513670.1:n.*69A=
ENST00000698340.1:c.552-193A=	ENSP00000513671.1:n.552-193A=
ENST00000162749.7:c.574A= MANE Select	ENSP00000162749.2:p.Thr192=
ENST00000162749.6:c.574A=	ENSP00000162749.2:p.Thr192=
ENST00000534885.5:c.*51A=	ENSP00000441803.1:n.*51A=
ENST00000535038.1:n.244A=
ENST00000536717.5:n.478A=
ENST00000537842.5:n.178A=
ENST00000539372.5:c.574A=	ENSP00000442059.1:p.Thr192=
ENST00000540022.5:c.445A=	ENSP00000438343.1:p.Thr149=
ENST00000543359.5:n.38-193A=
ENST00000543995.5:c.*161A=	ENSP00000442405.1:n.*161A=
NM_001065.3:c.574A= , LRG_193t1:c.574A=	NP_001056.1:p.Thr192=
NM_001346091.1:c.250A=	NP_001333020.1:p.Thr84=
NM_001346092.1:c.115A=	NP_001333021.1:p.Thr39=
NR_144351.1:n.855-193A=
NM_001065.4:c.574A= MANE Select	NP_001056.1:p.Thr192=
NM_001346091.2:c.250A=	NP_001333020.1:p.Thr84=
NM_001346092.2:c.115A=	NP_001333021.1:p.Thr39=
NR_144351.2:n.814-193A=