Canonical Allele Identifier: CA255743
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 11157
ClinVar RCV Id: RCV000011907
dbSNP Id: rs104894771

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659332G>C , CM000685.2:g.136659332G>C GRCh38
NC_000023.10:g.135741491G>C , CM000685.1:g.135741491G>C GRCh37
NC_000023.9:g.135569157G>C NCBI36
NG_007280.1:g.16156G>C , LRG_141:g.16156G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*321G>C ENSP00000512122.1:n.*321G>C
ENST00000695725.1:c.*258G>C ENSP00000512123.1:n.*258G>C
ENST00000695726.1:n.2671G>C
ENST00000695729.1:n.3506G>C
ENST00000370629.7:c.703G>C MANE Select ENSP00000359663.2:p.Ala235Pro
ENST00000370628.2:c.640G>C ENSP00000359662.2:p.Ala214Pro
ENST00000370629.6:c.703G>C ENSP00000359663.2:p.Ala235Pro
NM_000074.2:c.703G>C , LRG_141t1:c.703G>C NP_000065.1:p.Ala235Pro
NM_000074.3:c.703G>C MANE Select NP_000065.1:p.Ala235Pro