Canonical Allele Identifier: CA414756668
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659333C>G , CM000685.2:g.136659333C>G GRCh38
NC_000023.10:g.135741492C>G , CM000685.1:g.135741492C>G GRCh37
NC_000023.9:g.135569158C>G NCBI36
NG_007280.1:g.16157C>G , LRG_141:g.16157C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*322C>G ENSP00000512122.1:n.*322C>G
ENST00000695725.1:c.*259C>G ENSP00000512123.1:n.*259C>G
ENST00000695726.1:n.2672C>G
ENST00000695729.1:n.3507C>G
ENST00000370629.7:c.704C>G MANE Select ENSP00000359663.2:p.Ala235Gly
ENST00000370628.2:c.641C>G ENSP00000359662.2:p.Ala214Gly
ENST00000370629.6:c.704C>G ENSP00000359663.2:p.Ala235Gly
NM_000074.2:c.704C>G , LRG_141t1:c.704C>G NP_000065.1:p.Ala235Gly
NM_000074.3:c.704C>G MANE Select NP_000065.1:p.Ala235Gly