Canonical Allele Identifier: CA414752221
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648398G>T , CM000685.2:g.136648398G>T GRCh38
NC_000023.10:g.135730557G>T , CM000685.1:g.135730557G>T GRCh37
NC_000023.9:g.135558223G>T NCBI36
NG_007280.1:g.5222G>T , LRG_141:g.5222G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.150G>T ENSP00000512122.1:p.Leu50Phe
ENST00000695725.1:c.150G>T ENSP00000512123.1:p.Leu50Phe
ENST00000695726.1:n.193G>T
ENST00000695727.1:n.137G>T
ENST00000695728.1:n.137G>T
ENST00000370629.7:c.150G>T MANE Select ENSP00000359663.2:p.Leu50Phe
ENST00000370628.2:c.150G>T ENSP00000359662.2:p.Leu50Phe
ENST00000370629.6:c.150G>T ENSP00000359663.2:p.Leu50Phe
NM_000074.2:c.150G>T , LRG_141t1:c.150G>T NP_000065.1:p.Leu50Phe
NM_000074.3:c.150G>T MANE Select NP_000065.1:p.Leu50Phe