Canonical Allele Identifier: CA414756419
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741459A>G (hg19) chrX:g.136659300A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659300A>G , CM000685.2:g.136659300A>G GRCh38
NC_000023.10:g.135741459A>G , CM000685.1:g.135741459A>G GRCh37
NC_000023.9:g.135569125A>G NCBI36
NG_007280.1:g.16124A>G , LRG_141:g.16124A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*289A>G ENSP00000512122.1:n.*289A>G
ENST00000695725.1:c.*226A>G ENSP00000512123.1:n.*226A>G
ENST00000695726.1:n.2639A>G
ENST00000695729.1:n.3474A>G
ENST00000370629.7:c.671A>G MANE Select ENSP00000359663.2:p.His224Arg
ENST00000370628.2:c.608A>G ENSP00000359662.2:p.His203Arg
ENST00000370629.6:c.671A>G ENSP00000359663.2:p.His224Arg
NM_000074.2:c.671A>G , LRG_141t1:c.671A>G NP_000065.1:p.His224Arg
NM_000074.3:c.671A>G MANE Select NP_000065.1:p.His224Arg
Search 100 bp 5'
Search 100 bp 3'