Canonical Allele Identifier: CA414756679
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659336C>A , CM000685.2:g.136659336C>A GRCh38
NC_000023.10:g.135741495C>A , CM000685.1:g.135741495C>A GRCh37
NC_000023.9:g.135569161C>A NCBI36
NG_007280.1:g.16160C>A , LRG_141:g.16160C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*325C>A ENSP00000512122.1:n.*325C>A
ENST00000695725.1:c.*262C>A ENSP00000512123.1:n.*262C>A
ENST00000695726.1:n.2675C>A
ENST00000695729.1:n.3510C>A
ENST00000370629.7:c.707C>A MANE Select ENSP00000359663.2:p.Ser236Ter
ENST00000370628.2:c.644C>A ENSP00000359662.2:p.Ser215Ter
ENST00000370629.6:c.707C>A ENSP00000359663.2:p.Ser236Ter
NM_000074.2:c.707C>A , LRG_141t1:c.707C>A NP_000065.1:p.Ser236Ter
NM_000074.3:c.707C>A MANE Select NP_000065.1:p.Ser236Ter