Canonical Allele Identifier: CA2014022744
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6329821A= , CM000674.2:g.6329821A= GRCh38
NC_000012.11:g.6438987A= , CM000674.1:g.6438987A= GRCh37
NC_000012.10:g.6309248A= NCBI36
NG_007506.1:g.17275T= , LRG_193:g.17275T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.2115T=
ENST00000437813.8:c.*475T= ENSP00000513672.1:n.*475T=
ENST00000440083.7:c.1233T= ENSP00000413224.3:p.Leu411=
ENST00000535958.2:c.*841T= ENSP00000513673.1:n.*841T=
ENST00000698337.1:n.975T=
ENST00000698338.1:n.1628T=
ENST00000698339.1:c.*509T= ENSP00000513670.1:n.*509T=
ENST00000698340.1:c.*253T= ENSP00000513671.1:n.*253T=
ENST00000162749.7:c.1014T= MANE Select ENSP00000162749.2:p.Leu338=
ENST00000162749.6:c.1014T= ENSP00000162749.2:p.Leu338=
ENST00000534885.5:c.*491T= ENSP00000441803.1:n.*491T=
ENST00000536717.5:n.918T=
ENST00000540022.5:c.885T= ENSP00000438343.1:p.Leu295=
ENST00000543359.5:n.426T=
ENST00000543995.5:c.*601T= ENSP00000442405.1:n.*601T=
NM_001065.3:c.1014T= , LRG_193t1:c.1014T= NP_001056.1:p.Leu338=
NM_001346091.1:c.690T= NP_001333020.1:p.Leu230=
NM_001346092.1:c.555T= NP_001333021.1:p.Leu185=
NR_144351.1:n.1243T=
NM_001065.4:c.1014T= MANE Select NP_001056.1:p.Leu338=
NM_001346091.2:c.690T= NP_001333020.1:p.Leu230=
NM_001346092.2:c.555T= NP_001333021.1:p.Leu185=
NR_144351.2:n.1202T=