Canonical Allele Identifier: CA2460409211
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648519G= , CM000685.2:g.136648519G= GRCh38
NC_000023.10:g.135730678G= , CM000685.1:g.135730678G= GRCh37
NC_000023.9:g.135558344G= NCBI36
NG_007280.1:g.5343G= , LRG_141:g.5343G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.156+115G= ENSP00000512122.1:n.156+115G=
ENST00000695725.1:c.156+115G= ENSP00000512123.1:n.156+115G=
ENST00000695726.1:n.199+115G=
ENST00000695727.1:n.143+115G=
ENST00000695728.1:n.143+115G=
ENST00000370629.7:c.156+115G= MANE Select ENSP00000359663.2:n.156+115G=
ENST00000370628.2:c.156+115G= ENSP00000359662.2:n.156+115G=
ENST00000370629.6:c.156+115G= ENSP00000359663.2:n.156+115G=
NM_000074.2:c.156+115G= , LRG_141t1:c.156+115G= NP_000065.1:n.156+115G=
NM_000074.3:c.156+115G= MANE Select NP_000065.1:n.156+115G=