Canonical Allele Identifier: CA2695236796
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659289dup , CM000685.2:g.136659289dup GRCh38
NC_000023.10:g.135741448dup , CM000685.1:g.135741448dup GRCh37
NC_000023.9:g.135569114dup NCBI36
NG_007280.1:g.16113dup , LRG_141:g.16113dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*278dup ENSP00000512122.1:n.*278dup
ENST00000695725.1:c.*215dup ENSP00000512123.1:n.*215dup
ENST00000695726.1:n.2628dup
ENST00000695729.1:n.3463dup
ENST00000370629.7:c.660dup MANE Select ENSP00000359663.2:p.Gln221ThrfsTer10
ENST00000370628.2:c.597dup ENSP00000359662.2:p.Gln200ThrfsTer10
ENST00000370629.6:c.660dup ENSP00000359663.2:p.Gln221ThrfsTer10
NM_000074.2:c.660dup , LRG_141t1:c.660dup NP_000065.1:p.Gln221ThrfsTer10
NM_000074.3:c.660dup MANE Select NP_000065.1:p.Gln221ThrfsTer10