Canonical Allele Identifier: CA518856003
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741421C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659262C>G , CM000685.2:g.136659262C>G GRCh38
NC_000023.10:g.135741421C>G , CM000685.1:g.135741421C>G GRCh37
NC_000023.9:g.135569087C>G NCBI36
NG_007280.1:g.16086C>G , LRG_141:g.16086C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*251C>G ENSP00000512122.1:n.*251C>G
ENST00000695725.1:c.*188C>G ENSP00000512123.1:n.*188C>G
ENST00000695726.1:n.2601C>G
ENST00000695729.1:n.3436C>G
ENST00000370629.7:c.633C>G MANE Select ENSP00000359663.2:p.Thr211=
ENST00000370628.2:c.570C>G ENSP00000359662.2:p.Thr190=
ENST00000370629.6:c.633C>G ENSP00000359663.2:p.Thr211=
NM_000074.2:c.633C>G , LRG_141t1:c.633C>G NP_000065.1:p.Thr211=
NM_000074.3:c.633C>G MANE Select NP_000065.1:p.Thr211=
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