Canonical Allele Identifier: CA2014022746
Gene: TNFRSF1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6329823G= , CM000674.2:g.6329823G= GRCh38
NC_000012.11:g.6438989G= , CM000674.1:g.6438989G= GRCh37
NC_000012.10:g.6309250G= NCBI36
NG_007506.1:g.17273C= , LRG_193:g.17273C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366159.9:n.2113C=
ENST00000437813.8:c.*473C= ENSP00000513672.1:n.*473C=
ENST00000440083.7:c.1231C= ENSP00000413224.3:p.Leu411=
ENST00000535958.2:c.*839C= ENSP00000513673.1:n.*839C=
ENST00000698337.1:n.973C=
ENST00000698338.1:n.1626C=
ENST00000698339.1:c.*507C= ENSP00000513670.1:n.*507C=
ENST00000698340.1:c.*251C= ENSP00000513671.1:n.*251C=
ENST00000162749.7:c.1012C= MANE Select ENSP00000162749.2:p.Leu338=
ENST00000162749.6:c.1012C= ENSP00000162749.2:p.Leu338=
ENST00000534885.5:c.*489C= ENSP00000441803.1:n.*489C=
ENST00000536717.5:n.916C=
ENST00000540022.5:c.883C= ENSP00000438343.1:p.Leu295=
ENST00000543359.5:n.424C=
ENST00000543995.5:c.*599C= ENSP00000442405.1:n.*599C=
NM_001065.3:c.1012C= , LRG_193t1:c.1012C= NP_001056.1:p.Leu338=
NM_001346091.1:c.688C= NP_001333020.1:p.Leu230=
NM_001346092.1:c.553C= NP_001333021.1:p.Leu185=
NR_144351.1:n.1241C=
NM_001065.4:c.1012C= MANE Select NP_001056.1:p.Leu338=
NM_001346091.2:c.688C= NP_001333020.1:p.Leu230=
NM_001346092.2:c.553C= NP_001333021.1:p.Leu185=
NR_144351.2:n.1200C=