Canonical Allele Identifier: CA414753756
Community Standard Title: NM_000074.3(CD40LG):c.288+1G>A
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136650398G>A , CM000685.2:g.136650398G>A GRCh38
NC_000023.10:g.135732557G>A , CM000685.1:g.135732557G>A GRCh37
NC_000023.9:g.135560223G>A NCBI36
NG_007280.1:g.7222G>A , LRG_141:g.7222G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000074.3:c.288+1G>A MANE Select NP_000065.1:n.288+1G>A
ENST00000370629.7:c.288+1G>A MANE Select ENSP00000359663.2:n.288+1G>A
NM_000074.2:c.288+1G>A , LRG_141t1:c.288+1G>A NP_000065.1:n.288+1G>A
ENST00000370628.2:c.288+1G>A ENSP00000359662.2:n.288+1G>A
ENST00000370629.6:c.288+1G>A ENSP00000359663.2:n.288+1G>A
ENST00000695724.1:c.288+1G>A ENSP00000512122.1:n.288+1G>A
ENST00000695725.1:c.156+1994G>A ENSP00000512123.1:n.156+1994G>A
ENST00000695726.1:n.331+1G>A
ENST00000695727.1:n.275+1G>A
ENST00000695728.1:n.276G>A