Canonical Allele Identifier: CA2694819077
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659419G>C , CM000685.2:g.136659419G>C GRCh38
NC_000023.10:g.135741578G>C , CM000685.1:g.135741578G>C GRCh37
NC_000023.9:g.135569244G>C NCBI36
NG_007280.1:g.16243G>C , LRG_141:g.16243G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*408G>C ENSP00000512122.1:n.*408G>C
ENST00000695725.1:c.*345G>C ENSP00000512123.1:n.*345G>C
ENST00000695726.1:n.2758G>C
ENST00000695729.1:n.3593G>C
ENST00000370629.7:c.*4G>C MANE Select ENSP00000359663.2:n.*4G>C
ENST00000370628.2:c.*4G>C ENSP00000359662.2:n.*4G>C
ENST00000370629.6:c.*4G>C ENSP00000359663.2:n.*4G>C
NM_000074.2:c.*4G>C , LRG_141t1:c.*4G>C NP_000065.1:n.*4G>C
NM_000074.3:c.*4G>C MANE Select NP_000065.1:n.*4G>C