Canonical Allele Identifier: CA2014026081

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333468A= , CM000674.2:g.6333468A=	GRCh38
NC_000012.11:g.6442634A= , CM000674.1:g.6442634A=	GRCh37
NC_000012.10:g.6312895A=	NCBI36
NG_007506.1:g.13628T= , LRG_193:g.13628T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.405T=
ENST00000437813.8:c.371T=	ENSP00000513672.1:p.Val124=
ENST00000440083.7:c.371T=	ENSP00000413224.3:p.Val124=
ENST00000535958.2:c.*198T=	ENSP00000513673.1:n.*198T=
ENST00000698339.1:c.371T=	ENSP00000513670.1:p.Val124=
ENST00000698340.1:c.371T=	ENSP00000513671.1:p.Val124=
ENST00000162749.7:c.371T= MANE Select	ENSP00000162749.2:p.Val124=
ENST00000162749.6:c.371T=	ENSP00000162749.2:p.Val124=
ENST00000366159.8:c.371T=	ENSP00000380389.3:p.Val124=
ENST00000437813.7:n.332T=
ENST00000440083.6:c.371T=	ENSP00000413224.2:p.Val124=
ENST00000534885.5:c.217T=	ENSP00000441803.1:p.Cys73=
ENST00000536194.1:c.344T=	ENSP00000442919.1:p.Val115=
ENST00000539372.5:c.371T=	ENSP00000442059.1:p.Val124=
ENST00000540022.5:c.242T=	ENSP00000438343.1:p.Val81=
ENST00000543048.5:c.215-17T=	ENSP00000439981.1:n.215-17T=
ENST00000543995.5:c.194-17T=	ENSP00000442405.1:n.194-17T=
NM_001065.3:c.371T= , LRG_193t1:c.371T=	NP_001056.1:p.Val124=
NM_001346091.1:c.47T=	NP_001333020.1:p.Val16=
NM_001346092.1:c.-207T=	NP_001333021.1:n.-207T=
NR_144351.1:n.674T=
NM_001065.4:c.371T= MANE Select	NP_001056.1:p.Val124=
NM_001346091.2:c.47T=	NP_001333020.1:p.Val16=
NM_001346092.2:c.-207T=	NP_001333021.1:n.-207T=
NR_144351.2:n.633T=