Canonical Allele Identifier: CA2695236765
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659121_136659122dup , CM000685.2:g.136659121_136659122dup GRCh38
NC_000023.10:g.135741280_135741281dup , CM000685.1:g.135741280_135741281dup GRCh37
NC_000023.9:g.135568946_135568947dup NCBI36
NG_007280.1:g.15945_15946dup , LRG_141:g.15945_15946dup

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*110_*111dup ENSP00000512122.1:n.*110_*111dup
ENST00000695725.1:c.*47_*48dup ENSP00000512123.1:n.*47_*48dup
ENST00000695726.1:n.2460_2461dup
ENST00000695729.1:n.3295_3296dup
ENST00000370629.7:c.492_493dup MANE Select ENSP00000359663.2:p.Arg165LysfsTer27
ENST00000370628.2:c.429_430dup ENSP00000359662.2:p.Arg144LysfsTer27
ENST00000370629.6:c.492_493dup ENSP00000359663.2:p.Arg165LysfsTer27
NM_000074.2:c.492_493dup , LRG_141t1:c.492_493dup NP_000065.1:p.Arg165LysfsTer27
NM_000074.3:c.492_493dup MANE Select NP_000065.1:p.Arg165LysfsTer27