Canonical Allele Identifier: CA336267379
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs770475389

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136658960C>A , CM000685.2:g.136658960C>A GRCh38
NC_000023.10:g.135741119C>A , CM000685.1:g.135741119C>A GRCh37
NC_000023.9:g.135568785C>A NCBI36
NG_007280.1:g.15784C>A , LRG_141:g.15784C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*28-79C>A ENSP00000512122.1:n.*28-79C>A
ENST00000695725.1:c.157-79C>A ENSP00000512123.1:n.157-79C>A
ENST00000695726.1:n.2378-79C>A
ENST00000695729.1:n.3213-79C>A
ENST00000370629.7:c.410-79C>A MANE Select ENSP00000359663.2:n.410-79C>A
ENST00000370628.2:c.347-79C>A ENSP00000359662.2:n.347-79C>A
ENST00000370629.6:c.410-79C>A ENSP00000359663.2:n.410-79C>A
NM_000074.2:c.410-79C>A , LRG_141t1:c.410-79C>A NP_000065.1:n.410-79C>A
NM_000074.3:c.410-79C>A MANE Select NP_000065.1:n.410-79C>A