Canonical Allele Identifier: CA16608703
Community Standard Title: NM_000074.3(CD40LG):c.440C>A (p.Thr147Asn)
Gene: CD40LG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659069C>A , CM000685.2:g.136659069C>A GRCh38
NC_000023.10:g.135741228C>A , CM000685.1:g.135741228C>A GRCh37
NC_000023.9:g.135568894C>A NCBI36
NG_007280.1:g.15893C>A , LRG_141:g.15893C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000074.3:c.440C>A MANE Select NP_000065.1:p.Thr147Asn
ENST00000370629.7:c.440C>A MANE Select ENSP00000359663.2:p.Thr147Asn
NM_000074.2:c.440C>A , LRG_141t1:c.440C>A NP_000065.1:p.Thr147Asn
ENST00000370628.2:c.377C>A ENSP00000359662.2:p.Thr126Asn
ENST00000370629.6:c.440C>A ENSP00000359663.2:p.Thr147Asn
ENST00000695724.1:c.*58C>A ENSP00000512122.1:n.*58C>A
ENST00000695725.1:c.187C>A ENSP00000512123.1:p.Pro63Thr
ENST00000695726.1:n.2408C>A
ENST00000695729.1:n.3243C>A
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