Canonical Allele Identifier: CA2460412895
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659272G= , CM000685.2:g.136659272G= GRCh38
NC_000023.10:g.135741431G= , CM000685.1:g.135741431G= GRCh37
NC_000023.9:g.135569097G= NCBI36
NG_007280.1:g.16096G= , LRG_141:g.16096G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*261G= ENSP00000512122.1:n.*261G=
ENST00000695725.1:c.*198G= ENSP00000512123.1:n.*198G=
ENST00000695726.1:n.2611G=
ENST00000695729.1:n.3446G=
ENST00000370629.7:c.643G= MANE Select ENSP00000359663.2:p.Ala215=
ENST00000370628.2:c.580G= ENSP00000359662.2:p.Ala194=
ENST00000370629.6:c.643G= ENSP00000359663.2:p.Ala215=
NM_000074.2:c.643G= , LRG_141t1:c.643G= NP_000065.1:p.Ala215=
NM_000074.3:c.643G= MANE Select NP_000065.1:p.Ala215=