Canonical Allele Identifier: CA2579711988
Community Standard Title: NM_000074.3(CD40LG):c.289-27G>T
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136654346G>T , CM000685.2:g.136654346G>T GRCh38
NC_000023.10:g.135736505G>T , CM000685.1:g.135736505G>T GRCh37
NC_000023.9:g.135564171G>T NCBI36
NG_007280.1:g.11170G>T , LRG_141:g.11170G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000074.3:c.289-27G>T MANE Select NP_000065.1:n.289-27G>T
ENST00000370629.7:c.289-27G>T MANE Select ENSP00000359663.2:n.289-27G>T
NM_000074.2:c.289-27G>T , LRG_141t1:c.289-27G>T NP_000065.1:n.289-27G>T
ENST00000370628.2:c.289-27G>T ENSP00000359662.2:n.289-27G>T
ENST00000370629.6:c.289-27G>T ENSP00000359663.2:n.289-27G>T
ENST00000695724.1:c.289-2010G>T ENSP00000512122.1:n.289-2010G>T
ENST00000695725.1:c.157-4693G>T ENSP00000512123.1:n.157-4693G>T
ENST00000695726.1:n.332-27G>T
ENST00000695729.1:n.1140G>T