Canonical Allele Identifier: CA10590110

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 267318
• ClinVar RCV Id: RCV000258049
• dbSNP Id: rs886039866
• MyVariant Identifiers: chr12:g.6442542G>A (hg19) ; chr12:g.6333376G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333376G>A , CM000674.2:g.6333376G>A	GRCh38
NC_000012.11:g.6442542G>A , CM000674.1:g.6442542G>A	GRCh37
NC_000012.10:g.6312803G>A	NCBI36
NG_007506.1:g.13720C>T , LRG_193:g.13720C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.497C>T
ENST00000437813.8:c.463C>T	ENSP00000513672.1:p.His155Tyr
ENST00000440083.7:c.463C>T	ENSP00000413224.3:p.His155Tyr
ENST00000535958.2:c.*290C>T	ENSP00000513673.1:n.*290C>T
ENST00000698339.1:c.463C>T	ENSP00000513670.1:p.His155Tyr
ENST00000698340.1:c.463C>T	ENSP00000513671.1:p.His155Tyr
ENST00000162749.7:c.463C>T MANE Select	ENSP00000162749.2:p.His155Tyr
ENST00000162749.6:c.463C>T	ENSP00000162749.2:p.His155Tyr
ENST00000366159.8:c.463C>T	ENSP00000380389.3:p.His155Tyr
ENST00000437813.7:n.424C>T
ENST00000440083.6:c.463C>T	ENSP00000413224.2:p.His155Tyr
ENST00000534885.5:c.309C>T	ENSP00000441803.1:p.Cys103=
ENST00000537842.5:n.67C>T
ENST00000539372.5:c.463C>T	ENSP00000442059.1:p.His155Tyr
ENST00000540022.5:c.334C>T	ENSP00000438343.1:p.His112Tyr
ENST00000543048.5:c.*74C>T	ENSP00000439981.1:n.*74C>T
ENST00000543995.5:c.*50C>T	ENSP00000442405.1:n.*50C>T
NM_001065.3:c.463C>T , LRG_193t1:c.463C>T	NP_001056.1:p.His155Tyr
NM_001346091.1:c.139C>T	NP_001333020.1:p.His47Tyr
NM_001346092.1:c.-115C>T	NP_001333021.1:n.-115C>T
NR_144351.1:n.766C>T
NM_001065.4:c.463C>T MANE Select	NP_001056.1:p.His155Tyr
NM_001346091.2:c.139C>T	NP_001333020.1:p.His47Tyr
NM_001346092.2:c.-115C>T	NP_001333021.1:n.-115C>T
NR_144351.2:n.725C>T