Canonical Allele Identifier: CA280920

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 217017
• ClinVar RCV Id: RCV000200263 ; RCV000222279 ; RCV000487915 ; RCV001280954 ; RCV002262795
• dbSNP Id: rs4149584
• ExAC: 12:6442643 C / T
• gnomAD v2: 12-6442643-C-T
• gnomAD v3: 12-6333477-C-T
• gnomAD v4: 12-6333477-C-T
• MyVariant Identifiers: chr12:g.6442643C>T (hg19) ; chr12:g.6333477C>T (hg38)
• PubMed: PMID:25326637

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333477C>T , CM000674.2:g.6333477C>T	GRCh38
NC_000012.11:g.6442643C>T , CM000674.1:g.6442643C>T	GRCh37
NC_000012.10:g.6312904C>T	NCBI36
NG_007506.1:g.13619G>A , LRG_193:g.13619G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.396G>A
ENST00000437813.8:c.362G>A	ENSP00000513672.1:p.Arg121Gln
ENST00000440083.7:c.362G>A	ENSP00000413224.3:p.Arg121Gln
ENST00000535958.2:c.*189G>A	ENSP00000513673.1:n.*189G>A
ENST00000698339.1:c.362G>A	ENSP00000513670.1:p.Arg121Gln
ENST00000698340.1:c.362G>A	ENSP00000513671.1:p.Arg121Gln
ENST00000162749.7:c.362G>A MANE Select	ENSP00000162749.2:p.Arg121Gln
ENST00000162749.6:c.362G>A	ENSP00000162749.2:p.Arg121Gln
ENST00000366159.8:c.362G>A	ENSP00000380389.3:p.Arg121Gln
ENST00000437813.7:n.323G>A
ENST00000440083.6:c.362G>A	ENSP00000413224.2:p.Arg121Gln
ENST00000534885.5:c.208G>A	ENSP00000441803.1:p.Gly70Arg
ENST00000536194.1:c.335G>A	ENSP00000442919.1:p.Arg112Gln
ENST00000539372.5:c.362G>A	ENSP00000442059.1:p.Arg121Gln
ENST00000540022.5:c.233G>A	ENSP00000438343.1:p.Arg78Gln
ENST00000543048.5:c.215-26G>A	ENSP00000439981.1:n.215-26G>A
ENST00000543995.5:c.194-26G>A	ENSP00000442405.1:n.194-26G>A
NM_001065.3:c.362G>A , LRG_193t1:c.362G>A	NP_001056.1:p.Arg121Gln
NM_001346091.1:c.38G>A	NP_001333020.1:p.Arg13Gln
NM_001346092.1:c.-216G>A	NP_001333021.1:n.-216G>A
NR_144351.1:n.665G>A
NM_001065.4:c.362G>A MANE Select	NP_001056.1:p.Arg121Gln
NM_001346091.2:c.38G>A	NP_001333020.1:p.Arg13Gln
NM_001346092.2:c.-216G>A	NP_001333021.1:n.-216G>A
NR_144351.2:n.624G>A