Canonical Allele Identifier: CA383548989
Gene: TNFRSF1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6333071A>T , CM000674.2:g.6333071A>T GRCh38
NC_000012.11:g.6442237A>T , CM000674.1:g.6442237A>T GRCh37
NC_000012.10:g.6312498A>T NCBI36
NG_007506.1:g.14025T>A , LRG_193:g.14025T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.583T>A
ENST00000437813.8:c.549T>A ENSP00000513672.1:p.Ser183Arg
ENST00000440083.7:c.768T>A ENSP00000413224.3:p.Ser256Arg
ENST00000535958.2:c.*376T>A ENSP00000513673.1:n.*376T>A
ENST00000698339.1:c.549T>A ENSP00000513670.1:p.Ser183Arg
ENST00000698340.1:c.549T>A ENSP00000513671.1:p.Ser183Arg
ENST00000162749.7:c.549T>A MANE Select ENSP00000162749.2:p.Ser183Arg
ENST00000162749.6:c.549T>A ENSP00000162749.2:p.Ser183Arg
ENST00000366159.8:c.549T>A ENSP00000380389.3:p.Ser183Arg
ENST00000437813.7:n.510T>A
ENST00000534885.5:c.*26T>A ENSP00000441803.1:n.*26T>A
ENST00000537842.5:n.153T>A
ENST00000539372.5:c.549T>A ENSP00000442059.1:p.Ser183Arg
ENST00000540022.5:c.420T>A ENSP00000438343.1:p.Ser140Arg
ENST00000543048.5:c.*160T>A ENSP00000439981.1:n.*160T>A
ENST00000543359.5:n.35T>A
ENST00000543995.5:c.*136T>A ENSP00000442405.1:n.*136T>A
NM_001065.3:c.549T>A , LRG_193t1:c.549T>A NP_001056.1:p.Ser183Arg
NM_001346091.1:c.225T>A NP_001333020.1:p.Ser75Arg
NM_001346092.1:c.-29T>A NP_001333021.1:n.-29T>A
NR_144351.1:n.852T>A
NM_001065.4:c.549T>A MANE Select NP_001056.1:p.Ser183Arg
NM_001346091.2:c.225T>A NP_001333020.1:p.Ser75Arg
NM_001346092.2:c.-29T>A NP_001333021.1:n.-29T>A
NR_144351.2:n.811T>A