Canonical Allele Identifier: CA414757002
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659380A>T , CM000685.2:g.136659380A>T GRCh38
NC_000023.10:g.135741539A>T , CM000685.1:g.135741539A>T GRCh37
NC_000023.9:g.135569205A>T NCBI36
NG_007280.1:g.16204A>T , LRG_141:g.16204A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*369A>T ENSP00000512122.1:n.*369A>T
ENST00000695725.1:c.*306A>T ENSP00000512123.1:n.*306A>T
ENST00000695726.1:n.2719A>T
ENST00000695729.1:n.3554A>T
ENST00000370629.7:c.751A>T MANE Select ENSP00000359663.2:p.Thr251Ser
ENST00000370628.2:c.688A>T ENSP00000359662.2:p.Thr230Ser
ENST00000370629.6:c.751A>T ENSP00000359663.2:p.Thr251Ser
NM_000074.2:c.751A>T , LRG_141t1:c.751A>T NP_000065.1:p.Thr251Ser
NM_000074.3:c.751A>T MANE Select NP_000065.1:p.Thr251Ser