Canonical Allele Identifier: CA1137630137
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076128479

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659475A>G , CM000685.2:g.136659475A>G GRCh38
NC_000023.10:g.135741634A>G , CM000685.1:g.135741634A>G GRCh37
NC_000023.9:g.135569300A>G NCBI36
NG_007280.1:g.16299A>G , LRG_141:g.16299A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*464A>G ENSP00000512122.1:n.*464A>G
ENST00000695725.1:c.*401A>G ENSP00000512123.1:n.*401A>G
ENST00000695726.1:n.2814A>G
ENST00000695729.1:n.3649A>G
ENST00000370629.7:c.*60A>G MANE Select ENSP00000359663.2:n.*60A>G
ENST00000370628.2:c.*60A>G ENSP00000359662.2:n.*60A>G
ENST00000370629.6:c.*60A>G ENSP00000359663.2:n.*60A>G
NM_000074.2:c.*60A>G , LRG_141t1:c.*60A>G NP_000065.1:n.*60A>G
NM_000074.3:c.*60A>G MANE Select NP_000065.1:n.*60A>G