Canonical Allele Identifier: CA2014026495

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334436T= , CM000674.2:g.6334436T=	GRCh38
NC_000012.11:g.6443602T= , CM000674.1:g.6443602T=	GRCh37
NC_000012.10:g.6313863T=	NCBI36
NG_007506.1:g.12660A= , LRG_193:g.12660A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.74-192A=
ENST00000437813.8:c.40-192A=	ENSP00000513672.1:n.40-192A=
ENST00000440083.7:c.40-192A=	ENSP00000413224.3:n.40-192A=
ENST00000535958.2:c.40-192A=	ENSP00000513673.1:n.40-192A=
ENST00000698339.1:c.40-192A=	ENSP00000513670.1:n.40-192A=
ENST00000698340.1:c.40-192A=	ENSP00000513671.1:n.40-192A=
ENST00000162749.7:c.40-192A= MANE Select	ENSP00000162749.2:n.40-192A=
ENST00000162749.6:c.40-192A=	ENSP00000162749.2:n.40-192A=
ENST00000366159.8:c.40-192A=	ENSP00000380389.3:n.40-192A=
ENST00000440083.6:c.40-192A=	ENSP00000413224.2:n.40-192A=
ENST00000534885.5:c.40-571A=	ENSP00000441803.1:n.40-571A=
ENST00000535958.1:n.261-192A=
ENST00000536194.1:c.40-192A=	ENSP00000442919.1:n.40-192A=
ENST00000538363.1:n.230-192A=
ENST00000539372.5:c.40-192A=	ENSP00000442059.1:n.40-192A=
ENST00000540022.5:c.40-192A=	ENSP00000438343.1:n.40-192A=
ENST00000543048.5:c.40-192A=	ENSP00000439981.1:n.40-192A=
ENST00000543995.5:c.40-192A=	ENSP00000442405.1:n.40-192A=
NM_001065.3:c.40-192A= , LRG_193t1:c.40-192A=	NP_001056.1:n.40-192A=
NM_001346091.1:c.-131-571A=	NP_001333020.1:n.-131-571A=
NM_001346092.1:c.-538-192A=	NP_001333021.1:n.-538-192A=
NR_144351.1:n.343-192A=
NM_001065.4:c.40-192A= MANE Select	NP_001056.1:n.40-192A=
NM_001346091.2:c.-131-571A=	NP_001333020.1:n.-131-571A=
NM_001346092.2:c.-538-192A=	NP_001333021.1:n.-538-192A=
NR_144351.2:n.302-192A=