Canonical Allele Identifier: CA2460412889
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659261C= , CM000685.2:g.136659261C= GRCh38
NC_000023.10:g.135741420C= , CM000685.1:g.135741420C= GRCh37
NC_000023.9:g.135569086C= NCBI36
NG_007280.1:g.16085C= , LRG_141:g.16085C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*250C= ENSP00000512122.1:n.*250C=
ENST00000695725.1:c.*187C= ENSP00000512123.1:n.*187C=
ENST00000695726.1:n.2600C=
ENST00000695729.1:n.3435C=
ENST00000370629.7:c.632C= MANE Select ENSP00000359663.2:p.Thr211=
ENST00000370628.2:c.569C= ENSP00000359662.2:p.Thr190=
ENST00000370629.6:c.632C= ENSP00000359663.2:p.Thr211=
NM_000074.2:c.632C= , LRG_141t1:c.632C= NP_000065.1:p.Thr211=
NM_000074.3:c.632C= MANE Select NP_000065.1:p.Thr211=