Canonical Allele Identifier: CA6405614

Gene: TNFRSF1A

Linked Data

• ClinVar Variation Id: 1618501
• ClinVar RCV Id: RCV002082098 ; RCV002264464
• dbSNP Id: rs201015273
• ExAC: 12:6443399 C / T
• gnomAD v2: 12-6443399-C-T
• gnomAD v3: 12-6334233-C-T
• gnomAD v4: 12-6334233-C-T
• MyVariant Identifiers: chr12:g.6443399C>T (hg19) ; chr12:g.6334233C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6334233C>T , CM000674.2:g.6334233C>T	GRCh38
NC_000012.11:g.6443399C>T , CM000674.1:g.6443399C>T	GRCh37
NC_000012.10:g.6313660C>T	NCBI36
NG_007506.1:g.12863G>A , LRG_193:g.12863G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.85G>A
ENST00000437813.8:c.51G>A	ENSP00000513672.1:p.Glu17=
ENST00000440083.7:c.51G>A	ENSP00000413224.3:p.Glu17=
ENST00000535958.2:c.51G>A	ENSP00000513673.1:p.Glu17=
ENST00000698339.1:c.51G>A	ENSP00000513670.1:p.Glu17=
ENST00000698340.1:c.51G>A	ENSP00000513671.1:p.Glu17=
ENST00000162749.7:c.51G>A MANE Select	ENSP00000162749.2:p.Glu17=
ENST00000162749.6:c.51G>A	ENSP00000162749.2:p.Glu17=
ENST00000366159.8:c.51G>A	ENSP00000380389.3:p.Glu17=
ENST00000437813.7:n.12G>A
ENST00000440083.6:c.51G>A	ENSP00000413224.2:p.Glu17=
ENST00000534885.5:c.40-368G>A	ENSP00000441803.1:n.40-368G>A
ENST00000535958.1:n.272G>A
ENST00000536194.1:c.51G>A	ENSP00000442919.1:p.Glu17=
ENST00000538363.1:n.241G>A
ENST00000539372.5:c.51G>A	ENSP00000442059.1:p.Glu17=
ENST00000540022.5:c.51G>A	ENSP00000438343.1:p.Glu17=
ENST00000543048.5:c.51G>A	ENSP00000439981.1:p.Glu17=
ENST00000543995.5:c.51G>A	ENSP00000442405.1:p.Glu17=
NM_001065.3:c.51G>A , LRG_193t1:c.51G>A	NP_001056.1:p.Glu17=
NM_001346091.1:c.-131-368G>A	NP_001333020.1:n.-131-368G>A
NM_001346092.1:c.-527G>A	NP_001333021.1:n.-527G>A
NR_144351.1:n.354G>A
NM_001065.4:c.51G>A MANE Select	NP_001056.1:p.Glu17=
NM_001346091.2:c.-131-368G>A	NP_001333020.1:n.-131-368G>A
NM_001346092.2:c.-527G>A	NP_001333021.1:n.-527G>A
NR_144351.2:n.313G>A