Canonical Allele Identifier: CA2725532010
Gene: TNFRSF1A HGNC NCBI

Linked Data

dbSNP Id: rs2136822850

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333955A>G , CM000674.2:g.6333955A>G GRCh38
NC_000012.11:g.6443121A>G , CM000674.1:g.6443121A>G GRCh37
NC_000012.10:g.6313382A>G NCBI36
NG_007506.1:g.13141T>C , LRG_193:g.13141T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.228-90T>C
ENST00000437813.8:c.194-90T>C ENSP00000513672.1:n.194-90T>C
ENST00000440083.7:c.194-90T>C ENSP00000413224.3:n.194-90T>C
ENST00000535958.2:c.194-65T>C ENSP00000513673.1:n.194-65T>C
ENST00000698339.1:c.194-90T>C ENSP00000513670.1:n.194-90T>C
ENST00000698340.1:c.194-90T>C ENSP00000513671.1:n.194-90T>C
ENST00000162749.7:c.194-90T>C MANE Select ENSP00000162749.2:n.194-90T>C
ENST00000162749.6:c.194-90T>C ENSP00000162749.2:n.194-90T>C
ENST00000366159.8:c.194-90T>C ENSP00000380389.3:n.194-90T>C
ENST00000437813.7:n.155-90T>C
ENST00000440083.6:c.194-90T>C ENSP00000413224.2:n.194-90T>C
ENST00000534885.5:c.40-90T>C ENSP00000441803.1:n.40-90T>C
ENST00000535958.1:n.415-65T>C
ENST00000536194.1:c.194-117T>C ENSP00000442919.1:n.194-117T>C
ENST00000538363.1:n.519T>C
ENST00000539372.5:c.194-90T>C ENSP00000442059.1:n.194-90T>C
ENST00000540022.5:c.193+136T>C ENSP00000438343.1:n.193+136T>C
ENST00000543048.5:c.194-90T>C ENSP00000439981.1:n.194-90T>C
ENST00000543995.5:c.193+136T>C ENSP00000442405.1:n.193+136T>C
NM_001065.3:c.194-90T>C , LRG_193t1:c.194-90T>C NP_001056.1:n.194-90T>C
NM_001346091.1:c.-131-90T>C NP_001333020.1:n.-131-90T>C
NM_001346092.1:c.-384-90T>C NP_001333021.1:n.-384-90T>C
NR_144351.1:n.497-90T>C
NM_001065.4:c.194-90T>C MANE Select NP_001056.1:n.194-90T>C
NM_001346091.2:c.-131-90T>C NP_001333020.1:n.-131-90T>C
NM_001346092.2:c.-384-90T>C NP_001333021.1:n.-384-90T>C
NR_144351.2:n.456-90T>C