Canonical Allele Identifier: CA383548992
Gene: TNFRSF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333072C>T , CM000674.2:g.6333072C>T GRCh38
NC_000012.11:g.6442238C>T , CM000674.1:g.6442238C>T GRCh37
NC_000012.10:g.6312499C>T NCBI36
NG_007506.1:g.14024G>A , LRG_193:g.14024G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.582G>A
ENST00000437813.8:c.548G>A ENSP00000513672.1:p.Ser183Asn
ENST00000440083.7:c.767G>A ENSP00000413224.3:p.Ser256Asn
ENST00000535958.2:c.*375G>A ENSP00000513673.1:n.*375G>A
ENST00000698339.1:c.548G>A ENSP00000513670.1:p.Ser183Asn
ENST00000698340.1:c.548G>A ENSP00000513671.1:p.Ser183Asn
ENST00000162749.7:c.548G>A MANE Select ENSP00000162749.2:p.Ser183Asn
ENST00000162749.6:c.548G>A ENSP00000162749.2:p.Ser183Asn
ENST00000366159.8:c.548G>A ENSP00000380389.3:p.Ser183Asn
ENST00000437813.7:n.509G>A
ENST00000534885.5:c.*25G>A ENSP00000441803.1:n.*25G>A
ENST00000537842.5:n.152G>A
ENST00000539372.5:c.548G>A ENSP00000442059.1:p.Ser183Asn
ENST00000540022.5:c.419G>A ENSP00000438343.1:p.Ser140Asn
ENST00000543048.5:c.*159G>A ENSP00000439981.1:n.*159G>A
ENST00000543359.5:n.34G>A
ENST00000543995.5:c.*135G>A ENSP00000442405.1:n.*135G>A
NM_001065.3:c.548G>A , LRG_193t1:c.548G>A NP_001056.1:p.Ser183Asn
NM_001346091.1:c.224G>A NP_001333020.1:p.Ser75Asn
NM_001346092.1:c.-30G>A NP_001333021.1:n.-30G>A
NR_144351.1:n.851G>A
NM_001065.4:c.548G>A MANE Select NP_001056.1:p.Ser183Asn
NM_001346091.2:c.224G>A NP_001333020.1:p.Ser75Asn
NM_001346092.2:c.-30G>A NP_001333021.1:n.-30G>A
NR_144351.2:n.810G>A