Canonical Allele Identifier: CA414757169
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741561T>G (hg19) chrX:g.136659402T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659402T>G , CM000685.2:g.136659402T>G GRCh38
NC_000023.10:g.135741561T>G , CM000685.1:g.135741561T>G GRCh37
NC_000023.9:g.135569227T>G NCBI36
NG_007280.1:g.16226T>G , LRG_141:g.16226T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*391T>G ENSP00000512122.1:n.*391T>G
ENST00000695725.1:c.*328T>G ENSP00000512123.1:n.*328T>G
ENST00000695726.1:n.2741T>G
ENST00000695729.1:n.3576T>G
ENST00000370629.7:c.773T>G MANE Select ENSP00000359663.2:p.Leu258Ter
ENST00000370628.2:c.710T>G ENSP00000359662.2:p.Leu237Ter
ENST00000370629.6:c.773T>G ENSP00000359663.2:p.Leu258Ter
NM_000074.2:c.773T>G , LRG_141t1:c.773T>G NP_000065.1:p.Leu258Ter
NM_000074.3:c.773T>G MANE Select NP_000065.1:p.Leu258Ter
Search 100 bp 5'
Search 100 bp 3'