Canonical Allele Identifier: CA414756861
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659359C>G , CM000685.2:g.136659359C>G GRCh38
NC_000023.10:g.135741518C>G , CM000685.1:g.135741518C>G GRCh37
NC_000023.9:g.135569184C>G NCBI36
NG_007280.1:g.16183C>G , LRG_141:g.16183C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*348C>G ENSP00000512122.1:n.*348C>G
ENST00000695725.1:c.*285C>G ENSP00000512123.1:n.*285C>G
ENST00000695726.1:n.2698C>G
ENST00000695729.1:n.3533C>G
ENST00000370629.7:c.730C>G MANE Select ENSP00000359663.2:p.Pro244Ala
ENST00000370628.2:c.667C>G ENSP00000359662.2:p.Pro223Ala
ENST00000370629.6:c.730C>G ENSP00000359663.2:p.Pro244Ala
NM_000074.2:c.730C>G , LRG_141t1:c.730C>G NP_000065.1:p.Pro244Ala
NM_000074.3:c.730C>G MANE Select NP_000065.1:p.Pro244Ala