Canonical Allele Identifier: CA2694819083
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659442G>C , CM000685.2:g.136659442G>C GRCh38
NC_000023.10:g.135741601G>C , CM000685.1:g.135741601G>C GRCh37
NC_000023.9:g.135569267G>C NCBI36
NG_007280.1:g.16266G>C , LRG_141:g.16266G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*431G>C ENSP00000512122.1:n.*431G>C
ENST00000695725.1:c.*368G>C ENSP00000512123.1:n.*368G>C
ENST00000695726.1:n.2781G>C
ENST00000695729.1:n.3616G>C
ENST00000370629.7:c.*27G>C MANE Select ENSP00000359663.2:n.*27G>C
ENST00000370628.2:c.*27G>C ENSP00000359662.2:n.*27G>C
ENST00000370629.6:c.*27G>C ENSP00000359663.2:n.*27G>C
NM_000074.2:c.*27G>C , LRG_141t1:c.*27G>C NP_000065.1:n.*27G>C
NM_000074.3:c.*27G>C MANE Select NP_000065.1:n.*27G>C