Canonical Allele Identifier: CA383547761

Gene: TNFRSF1A

Linked Data

• MyVariant Identifiers: chr12:g.6439844A>T (hg19) ; chr12:g.6330678A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6330678A>T , CM000674.2:g.6330678A>T	GRCh38
NC_000012.11:g.6439844A>T , CM000674.1:g.6439844A>T	GRCh37
NC_000012.10:g.6310105A>T	NCBI36
NG_007506.1:g.16418T>A , LRG_193:g.16418T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.1760T>A
ENST00000437813.8:c.*120T>A	ENSP00000513672.1:n.*120T>A
ENST00000440083.7:c.878T>A	ENSP00000413224.3:p.Phe293Tyr
ENST00000535038.2:n.841T>A
ENST00000535958.2:c.*486T>A	ENSP00000513673.1:n.*486T>A
ENST00000698337.1:n.649T>A
ENST00000698338.1:n.1073T>A
ENST00000698339.1:c.*154T>A	ENSP00000513670.1:n.*154T>A
ENST00000698340.1:c.585T>A	ENSP00000513671.1:p.Leu195=
ENST00000162749.7:c.659T>A MANE Select	ENSP00000162749.2:p.Phe220Tyr
ENST00000162749.6:c.659T>A	ENSP00000162749.2:p.Phe220Tyr
ENST00000534885.5:c.*136T>A	ENSP00000441803.1:n.*136T>A
ENST00000535038.1:n.470T>A
ENST00000536717.5:n.563T>A
ENST00000537842.5:n.263T>A
ENST00000539372.5:c.659T>A	ENSP00000442059.1:p.Phe220Tyr
ENST00000540022.5:c.530T>A	ENSP00000438343.1:p.Phe177Tyr
ENST00000543359.5:n.71T>A
ENST00000543995.5:c.*246T>A	ENSP00000442405.1:n.*246T>A
NM_001065.3:c.659T>A , LRG_193t1:c.659T>A	NP_001056.1:p.Phe220Tyr
NM_001346091.1:c.335T>A	NP_001333020.1:p.Phe112Tyr
NM_001346092.1:c.200T>A	NP_001333021.1:p.Phe67Tyr
NR_144351.1:n.888T>A
NM_001065.4:c.659T>A MANE Select	NP_001056.1:p.Phe220Tyr
NM_001346091.2:c.335T>A	NP_001333020.1:p.Phe112Tyr
NM_001346092.2:c.200T>A	NP_001333021.1:p.Phe67Tyr
NR_144351.2:n.847T>A