Canonical Allele Identifier: CA383550264
Gene: TNFRSF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333493A>C , CM000674.2:g.6333493A>C GRCh38
NC_000012.11:g.6442659A>C , CM000674.1:g.6442659A>C GRCh37
NC_000012.10:g.6312920A>C NCBI36
NG_007506.1:g.13603T>G , LRG_193:g.13603T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366159.9:n.380T>G
ENST00000437813.8:c.346T>G ENSP00000513672.1:p.Ser116Ala
ENST00000440083.7:c.346T>G ENSP00000413224.3:p.Ser116Ala
ENST00000535958.2:c.*173T>G ENSP00000513673.1:n.*173T>G
ENST00000698339.1:c.346T>G ENSP00000513670.1:p.Ser116Ala
ENST00000698340.1:c.346T>G ENSP00000513671.1:p.Ser116Ala
ENST00000162749.7:c.346T>G MANE Select ENSP00000162749.2:p.Ser116Ala
ENST00000162749.6:c.346T>G ENSP00000162749.2:p.Ser116Ala
ENST00000366159.8:c.346T>G ENSP00000380389.3:p.Ser116Ala
ENST00000437813.7:n.307T>G
ENST00000440083.6:c.346T>G ENSP00000413224.2:p.Ser116Ala
ENST00000534885.5:c.192T>G ENSP00000441803.1:p.Leu64=
ENST00000536194.1:c.319T>G ENSP00000442919.1:p.Ser107Ala
ENST00000539372.5:c.346T>G ENSP00000442059.1:p.Ser116Ala
ENST00000540022.5:c.217T>G ENSP00000438343.1:p.Ser73Ala
ENST00000543048.5:c.215-42T>G ENSP00000439981.1:n.215-42T>G
ENST00000543995.5:c.194-42T>G ENSP00000442405.1:n.194-42T>G
NM_001065.3:c.346T>G , LRG_193t1:c.346T>G NP_001056.1:p.Ser116Ala
NM_001346091.1:c.22T>G NP_001333020.1:p.Ser8Ala
NM_001346092.1:c.-232T>G NP_001333021.1:n.-232T>G
NR_144351.1:n.649T>G
NM_001065.4:c.346T>G MANE Select NP_001056.1:p.Ser116Ala
NM_001346091.2:c.22T>G NP_001333020.1:p.Ser8Ala
NM_001346092.2:c.-232T>G NP_001333021.1:n.-232T>G
NR_144351.2:n.608T>G