Canonical Allele Identifier: CA2014026306

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333921A= , CM000674.2:g.6333921A=	GRCh38
NC_000012.11:g.6443087A= , CM000674.1:g.6443087A=	GRCh37
NC_000012.10:g.6313348A=	NCBI36
NG_007506.1:g.13175T= , LRG_193:g.13175T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.228-56T=
ENST00000437813.8:c.194-56T=	ENSP00000513672.1:n.194-56T=
ENST00000440083.7:c.194-56T=	ENSP00000413224.3:n.194-56T=
ENST00000535958.2:c.194-31T=	ENSP00000513673.1:n.194-31T=
ENST00000698339.1:c.194-56T=	ENSP00000513670.1:n.194-56T=
ENST00000698340.1:c.194-56T=	ENSP00000513671.1:n.194-56T=
ENST00000162749.7:c.194-56T= MANE Select	ENSP00000162749.2:n.194-56T=
ENST00000162749.6:c.194-56T=	ENSP00000162749.2:n.194-56T=
ENST00000366159.8:c.194-56T=	ENSP00000380389.3:n.194-56T=
ENST00000437813.7:n.155-56T=
ENST00000440083.6:c.194-56T=	ENSP00000413224.2:n.194-56T=
ENST00000534885.5:c.40-56T=	ENSP00000441803.1:n.40-56T=
ENST00000535958.1:n.415-31T=
ENST00000536194.1:c.194-83T=	ENSP00000442919.1:n.194-83T=
ENST00000538363.1:n.553T=
ENST00000539372.5:c.194-56T=	ENSP00000442059.1:n.194-56T=
ENST00000540022.5:c.193+170T=	ENSP00000438343.1:n.193+170T=
ENST00000543048.5:c.194-56T=	ENSP00000439981.1:n.194-56T=
ENST00000543995.5:c.193+170T=	ENSP00000442405.1:n.193+170T=
NM_001065.3:c.194-56T= , LRG_193t1:c.194-56T=	NP_001056.1:n.194-56T=
NM_001346091.1:c.-131-56T=	NP_001333020.1:n.-131-56T=
NM_001346092.1:c.-384-56T=	NP_001333021.1:n.-384-56T=
NR_144351.1:n.497-56T=
NM_001065.4:c.194-56T= MANE Select	NP_001056.1:n.194-56T=
NM_001346091.2:c.-131-56T=	NP_001333020.1:n.-131-56T=
NM_001346092.2:c.-384-56T=	NP_001333021.1:n.-384-56T=
NR_144351.2:n.456-56T=