Canonical Allele Identifier: CA383550552

Gene: TNFRSF1A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333794A>T , CM000674.2:g.6333794A>T	GRCh38
NC_000012.11:g.6442960A>T , CM000674.1:g.6442960A>T	GRCh37
NC_000012.10:g.6313221A>T	NCBI36
NG_007506.1:g.13302T>A , LRG_193:g.13302T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.299T>A
ENST00000437813.8:c.265T>A	ENSP00000513672.1:p.Phe89Ile
ENST00000440083.7:c.265T>A	ENSP00000413224.3:p.Phe89Ile
ENST00000535958.2:c.*92T>A	ENSP00000513673.1:n.*92T>A
ENST00000698339.1:c.265T>A	ENSP00000513670.1:p.Phe89Ile
ENST00000698340.1:c.265T>A	ENSP00000513671.1:p.Phe89Ile
ENST00000162749.7:c.265T>A MANE Select	ENSP00000162749.2:p.Phe89Ile
ENST00000162749.6:c.265T>A	ENSP00000162749.2:p.Phe89Ile
ENST00000366159.8:c.265T>A	ENSP00000380389.3:p.Phe89Ile
ENST00000437813.7:n.226T>A
ENST00000440083.6:c.265T>A	ENSP00000413224.2:p.Phe89Ile
ENST00000534885.5:c.111T>A	ENSP00000441803.1:p.Pro37=
ENST00000535958.1:n.511T>A
ENST00000536194.1:c.238T>A	ENSP00000442919.1:p.Phe80Ile
ENST00000539372.5:c.265T>A	ENSP00000442059.1:p.Phe89Ile
ENST00000540022.5:c.194-278T>A	ENSP00000438343.1:n.194-278T>A
ENST00000543048.5:c.214+51T>A	ENSP00000439981.1:n.214+51T>A
ENST00000543995.5:c.193+297T>A	ENSP00000442405.1:n.193+297T>A
NM_001065.3:c.265T>A , LRG_193t1:c.265T>A	NP_001056.1:p.Phe89Ile
NM_001346091.1:c.-60T>A	NP_001333020.1:n.-60T>A
NM_001346092.1:c.-313T>A	NP_001333021.1:n.-313T>A
NR_144351.1:n.568T>A
NM_001065.4:c.265T>A MANE Select	NP_001056.1:p.Phe89Ile
NM_001346091.2:c.-60T>A	NP_001333020.1:n.-60T>A
NM_001346092.2:c.-313T>A	NP_001333021.1:n.-313T>A
NR_144351.2:n.527T>A