Canonical Allele Identifier: CA603483377

Gene: TNFRSF1A

Linked Data

• dbSNP Id: rs1254327488
• gnomAD v2: 12-6442353-T-G
• gnomAD v4: 12-6333187-T-G
• MyVariant Identifiers: chr12:g.6442353T>G (hg19) ; chr12:g.6333187T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333187T>G , CM000674.2:g.6333187T>G	GRCh38
NC_000012.11:g.6442353T>G , CM000674.1:g.6442353T>G	GRCh37
NC_000012.10:g.6312614T>G	NCBI36
NG_007506.1:g.13909A>C , LRG_193:g.13909A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.507-40A>C
ENST00000437813.8:c.473-40A>C	ENSP00000513672.1:n.473-40A>C
ENST00000440083.7:c.652A>C	ENSP00000413224.3:p.Arg218=
ENST00000535958.2:c.*300-40A>C	ENSP00000513673.1:n.*300-40A>C
ENST00000698339.1:c.473-40A>C	ENSP00000513670.1:n.473-40A>C
ENST00000698340.1:c.473-40A>C	ENSP00000513671.1:n.473-40A>C
ENST00000162749.7:c.473-40A>C MANE Select	ENSP00000162749.2:n.473-40A>C
ENST00000162749.6:c.473-40A>C	ENSP00000162749.2:n.473-40A>C
ENST00000366159.8:c.473-40A>C	ENSP00000380389.3:n.473-40A>C
ENST00000437813.7:n.434-40A>C
ENST00000440083.6:c.652A>C	ENSP00000413224.2:p.Arg218=
ENST00000534885.5:c.319-40A>C	ENSP00000441803.1:n.319-40A>C
ENST00000537842.5:n.77-40A>C
ENST00000539372.5:c.473-40A>C	ENSP00000442059.1:n.473-40A>C
ENST00000540022.5:c.344-40A>C	ENSP00000438343.1:n.344-40A>C
ENST00000543048.5:c.*84-40A>C	ENSP00000439981.1:n.*84-40A>C
ENST00000543995.5:c.*60-40A>C	ENSP00000442405.1:n.*60-40A>C
NM_001065.3:c.473-40A>C , LRG_193t1:c.473-40A>C	NP_001056.1:n.473-40A>C
NM_001346091.1:c.149-40A>C	NP_001333020.1:n.149-40A>C
NM_001346092.1:c.-105-40A>C	NP_001333021.1:n.-105-40A>C
NR_144351.1:n.776-40A>C
NM_001065.4:c.473-40A>C MANE Select	NP_001056.1:n.473-40A>C
NM_001346091.2:c.149-40A>C	NP_001333020.1:n.149-40A>C
NM_001346092.2:c.-105-40A>C	NP_001333021.1:n.-105-40A>C
NR_144351.2:n.735-40A>C