Canonical Allele Identifier: CA2014026229

Gene: TNFRSF1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333772A= , CM000674.2:g.6333772A=	GRCh38
NC_000012.11:g.6442938A= , CM000674.1:g.6442938A=	GRCh37
NC_000012.10:g.6313199A=	NCBI36
NG_007506.1:g.13324T= , LRG_193:g.13324T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366159.9:n.321T=
ENST00000437813.8:c.287T=	ENSP00000513672.1:p.Leu96=
ENST00000440083.7:c.287T=	ENSP00000413224.3:p.Leu96=
ENST00000535958.2:c.*114T=	ENSP00000513673.1:n.*114T=
ENST00000698339.1:c.287T=	ENSP00000513670.1:p.Leu96=
ENST00000698340.1:c.287T=	ENSP00000513671.1:p.Leu96=
ENST00000162749.7:c.287T= MANE Select	ENSP00000162749.2:p.Leu96=
ENST00000162749.6:c.287T=	ENSP00000162749.2:p.Leu96=
ENST00000366159.8:c.287T=	ENSP00000380389.3:p.Leu96=
ENST00000437813.7:n.248T=
ENST00000440083.6:c.287T=	ENSP00000413224.2:p.Leu96=
ENST00000534885.5:c.133T=	ENSP00000441803.1:p.Ser45=
ENST00000535958.1:n.533T=
ENST00000536194.1:c.260T=	ENSP00000442919.1:p.Leu87=
ENST00000539372.5:c.287T=	ENSP00000442059.1:p.Leu96=
ENST00000540022.5:c.194-256T=	ENSP00000438343.1:n.194-256T=
ENST00000543048.5:c.214+73T=	ENSP00000439981.1:n.214+73T=
ENST00000543995.5:c.193+319T=	ENSP00000442405.1:n.193+319T=
NM_001065.3:c.287T= , LRG_193t1:c.287T=	NP_001056.1:p.Leu96=
NM_001346091.1:c.-38T=	NP_001333020.1:n.-38T=
NM_001346092.1:c.-291T=	NP_001333021.1:n.-291T=
NR_144351.1:n.590T=
NM_001065.4:c.287T= MANE Select	NP_001056.1:p.Leu96=
NM_001346091.2:c.-38T=	NP_001333020.1:n.-38T=
NM_001346092.2:c.-291T=	NP_001333021.1:n.-291T=
NR_144351.2:n.549T=