Canonical Allele Identifier: CA2014026245

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333800C= , CM000674.2:g.6333800C=	GRCh38
NC_000012.11:g.6442966C= , CM000674.1:g.6442966C=	GRCh37
NC_000012.10:g.6313227C=	NCBI36
NG_007506.1:g.13296G= , LRG_193:g.13296G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.293G=
ENST00000437813.8:c.259G=	ENSP00000513672.1:p.Gly87=
ENST00000440083.7:c.259G=	ENSP00000413224.3:p.Gly87=
ENST00000535958.2:c.*86G=	ENSP00000513673.1:n.*86G=
ENST00000698339.1:c.259G=	ENSP00000513670.1:p.Gly87=
ENST00000698340.1:c.259G=	ENSP00000513671.1:p.Gly87=
ENST00000162749.7:c.259G= MANE Select	ENSP00000162749.2:p.Gly87=
ENST00000162749.6:c.259G=	ENSP00000162749.2:p.Gly87=
ENST00000366159.8:c.259G=	ENSP00000380389.3:p.Gly87=
ENST00000437813.7:n.220G=
ENST00000440083.6:c.259G=	ENSP00000413224.2:p.Gly87=
ENST00000534885.5:c.105G=	ENSP00000441803.1:p.Ala35=
ENST00000535958.1:n.505G=
ENST00000536194.1:c.232G=	ENSP00000442919.1:p.Gly78=
ENST00000539372.5:c.259G=	ENSP00000442059.1:p.Gly87=
ENST00000540022.5:c.194-284G=	ENSP00000438343.1:n.194-284G=
ENST00000543048.5:c.214+45G=	ENSP00000439981.1:n.214+45G=
ENST00000543995.5:c.193+291G=	ENSP00000442405.1:n.193+291G=
NM_001065.3:c.259G= , LRG_193t1:c.259G=	NP_001056.1:p.Gly87=
NM_001346091.1:c.-66G=	NP_001333020.1:n.-66G=
NM_001346092.1:c.-319G=	NP_001333021.1:n.-319G=
NR_144351.1:n.562G=
NM_001065.4:c.259G= MANE Select	NP_001056.1:p.Gly87=
NM_001346091.2:c.-66G=	NP_001333020.1:n.-66G=
NM_001346092.2:c.-319G=	NP_001333021.1:n.-319G=
NR_144351.2:n.521G=