Canonical Allele Identifier: CA414756765
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659347A>T , CM000685.2:g.136659347A>T GRCh38
NC_000023.10:g.135741506A>T , CM000685.1:g.135741506A>T GRCh37
NC_000023.9:g.135569172A>T NCBI36
NG_007280.1:g.16171A>T , LRG_141:g.16171A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*336A>T ENSP00000512122.1:n.*336A>T
ENST00000695725.1:c.*273A>T ENSP00000512123.1:n.*273A>T
ENST00000695726.1:n.2686A>T
ENST00000695729.1:n.3521A>T
ENST00000370629.7:c.718A>T MANE Select ENSP00000359663.2:p.Asn240Tyr
ENST00000370628.2:c.655A>T ENSP00000359662.2:p.Asn219Tyr
ENST00000370629.6:c.718A>T ENSP00000359663.2:p.Asn240Tyr
NM_000074.2:c.718A>T , LRG_141t1:c.718A>T NP_000065.1:p.Asn240Tyr
NM_000074.3:c.718A>T MANE Select NP_000065.1:p.Asn240Tyr