Canonical Allele Identifier: CA414756311
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659275A>T , CM000685.2:g.136659275A>T GRCh38
NC_000023.10:g.135741434A>T , CM000685.1:g.135741434A>T GRCh37
NC_000023.9:g.135569100A>T NCBI36
NG_007280.1:g.16099A>T , LRG_141:g.16099A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*264A>T ENSP00000512122.1:n.*264A>T
ENST00000695725.1:c.*201A>T ENSP00000512123.1:n.*201A>T
ENST00000695726.1:n.2614A>T
ENST00000695729.1:n.3449A>T
ENST00000370629.7:c.646A>T MANE Select ENSP00000359663.2:p.Lys216Ter
ENST00000370628.2:c.583A>T ENSP00000359662.2:p.Lys195Ter
ENST00000370629.6:c.646A>T ENSP00000359663.2:p.Lys216Ter
NM_000074.2:c.646A>T , LRG_141t1:c.646A>T NP_000065.1:p.Lys216Ter
NM_000074.3:c.646A>T MANE Select NP_000065.1:p.Lys216Ter