Canonical Allele Identifier: CA6405517

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs750056341
• ExAC: 12:6442408 A / G
• gnomAD v2: 12-6442408-A-G
• gnomAD v3: 12-6333242-A-G
• gnomAD v4: 12-6333242-A-G
• MyVariant Identifiers: chr12:g.6442408A>G (hg19) ; chr12:g.6333242A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333242A>G , CM000674.2:g.6333242A>G	GRCh38
NC_000012.11:g.6442408A>G , CM000674.1:g.6442408A>G	GRCh37
NC_000012.10:g.6312669A>G	NCBI36
NG_007506.1:g.13854T>C , LRG_193:g.13854T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.507-95T>C
ENST00000437813.8:c.473-95T>C	ENSP00000513672.1:n.473-95T>C
ENST00000440083.7:c.597T>C	ENSP00000413224.3:p.Ser199=
ENST00000535958.2:c.*300-95T>C	ENSP00000513673.1:n.*300-95T>C
ENST00000698339.1:c.473-95T>C	ENSP00000513670.1:n.473-95T>C
ENST00000698340.1:c.473-95T>C	ENSP00000513671.1:n.473-95T>C
ENST00000162749.7:c.473-95T>C MANE Select	ENSP00000162749.2:n.473-95T>C
ENST00000162749.6:c.473-95T>C	ENSP00000162749.2:n.473-95T>C
ENST00000366159.8:c.473-95T>C	ENSP00000380389.3:n.473-95T>C
ENST00000437813.7:n.434-95T>C
ENST00000440083.6:c.597T>C	ENSP00000413224.2:p.Ser199=
ENST00000534885.5:c.319-95T>C	ENSP00000441803.1:n.319-95T>C
ENST00000537842.5:n.77-95T>C
ENST00000539372.5:c.473-95T>C	ENSP00000442059.1:n.473-95T>C
ENST00000540022.5:c.344-95T>C	ENSP00000438343.1:n.344-95T>C
ENST00000543048.5:c.*84-95T>C	ENSP00000439981.1:n.*84-95T>C
ENST00000543995.5:c.*60-95T>C	ENSP00000442405.1:n.*60-95T>C
NM_001065.3:c.473-95T>C , LRG_193t1:c.473-95T>C	NP_001056.1:n.473-95T>C
NM_001346091.1:c.149-95T>C	NP_001333020.1:n.149-95T>C
NM_001346092.1:c.-105-95T>C	NP_001333021.1:n.-105-95T>C
NR_144351.1:n.776-95T>C
NM_001065.4:c.473-95T>C MANE Select	NP_001056.1:n.473-95T>C
NM_001346091.2:c.149-95T>C	NP_001333020.1:n.149-95T>C
NM_001346092.2:c.-105-95T>C	NP_001333021.1:n.-105-95T>C
NR_144351.2:n.735-95T>C