Canonical Allele Identifier: CA518856008
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741430C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659271C>G , CM000685.2:g.136659271C>G GRCh38
NC_000023.10:g.135741430C>G , CM000685.1:g.135741430C>G GRCh37
NC_000023.9:g.135569096C>G NCBI36
NG_007280.1:g.16095C>G , LRG_141:g.16095C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*260C>G ENSP00000512122.1:n.*260C>G
ENST00000695725.1:c.*197C>G ENSP00000512123.1:n.*197C>G
ENST00000695726.1:n.2610C>G
ENST00000695729.1:n.3445C>G
ENST00000370629.7:c.642C>G MANE Select ENSP00000359663.2:p.Ser214=
ENST00000370628.2:c.579C>G ENSP00000359662.2:p.Ser193=
ENST00000370629.6:c.642C>G ENSP00000359663.2:p.Ser214=
NM_000074.2:c.642C>G , LRG_141t1:c.642C>G NP_000065.1:p.Ser214=
NM_000074.3:c.642C>G MANE Select NP_000065.1:p.Ser214=
Search 100 bp 5'
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