Canonical Allele Identifier: CA280849

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 97698
• ClinVar RCV Id: RCV000083951
• dbSNP Id: rs104895242
• MyVariant Identifiers: chr12:g.6442625C>T (hg19) ; chr12:g.6333459C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333459C>T , CM000674.2:g.6333459C>T	GRCh38
NC_000012.11:g.6442625C>T , CM000674.1:g.6442625C>T	GRCh37
NC_000012.10:g.6312886C>T	NCBI36
NG_007506.1:g.13637G>A , LRG_193:g.13637G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.414G>A
ENST00000437813.8:c.380G>A	ENSP00000513672.1:p.Cys127Tyr
ENST00000440083.7:c.380G>A	ENSP00000413224.3:p.Cys127Tyr
ENST00000535958.2:c.*207G>A	ENSP00000513673.1:n.*207G>A
ENST00000698339.1:c.380G>A	ENSP00000513670.1:p.Cys127Tyr
ENST00000698340.1:c.380G>A	ENSP00000513671.1:p.Cys127Tyr
ENST00000162749.7:c.380G>A MANE Select	ENSP00000162749.2:p.Cys127Tyr
ENST00000162749.6:c.380G>A	ENSP00000162749.2:p.Cys127Tyr
ENST00000366159.8:c.380G>A	ENSP00000380389.3:p.Cys127Tyr
ENST00000437813.7:n.341G>A
ENST00000440083.6:c.380G>A	ENSP00000413224.2:p.Cys127Tyr
ENST00000534885.5:c.226G>A	ENSP00000441803.1:p.Ala76Thr
ENST00000536194.1:c.353G>A	ENSP00000442919.1:p.Cys118Tyr
ENST00000539372.5:c.380G>A	ENSP00000442059.1:p.Cys127Tyr
ENST00000540022.5:c.251G>A	ENSP00000438343.1:p.Cys84Tyr
ENST00000543048.5:c.215-8G>A	ENSP00000439981.1:n.215-8G>A
ENST00000543995.5:c.194-8G>A	ENSP00000442405.1:n.194-8G>A
NM_001065.3:c.380G>A , LRG_193t1:c.380G>A	NP_001056.1:p.Cys127Tyr
NM_001346091.1:c.56G>A	NP_001333020.1:p.Cys19Tyr
NM_001346092.1:c.-198G>A	NP_001333021.1:n.-198G>A
NR_144351.1:n.683G>A
NM_001065.4:c.380G>A MANE Select	NP_001056.1:p.Cys127Tyr
NM_001346091.2:c.56G>A	NP_001333020.1:p.Cys19Tyr
NM_001346092.2:c.-198G>A	NP_001333021.1:n.-198G>A
NR_144351.2:n.642G>A