Canonical Allele Identifier: CA336267484
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs893448151

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659482A>C , CM000685.2:g.136659482A>C GRCh38
NC_000023.10:g.135741641A>C , CM000685.1:g.135741641A>C GRCh37
NC_000023.9:g.135569307A>C NCBI36
NG_007280.1:g.16306A>C , LRG_141:g.16306A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*471A>C ENSP00000512122.1:n.*471A>C
ENST00000695725.1:c.*408A>C ENSP00000512123.1:n.*408A>C
ENST00000695726.1:n.2821A>C
ENST00000695729.1:n.3656A>C
ENST00000370629.7:c.*67A>C MANE Select ENSP00000359663.2:n.*67A>C
ENST00000370628.2:c.*67A>C ENSP00000359662.2:n.*67A>C
ENST00000370629.6:c.*67A>C ENSP00000359663.2:n.*67A>C
NM_000074.2:c.*67A>C , LRG_141t1:c.*67A>C NP_000065.1:n.*67A>C
NM_000074.3:c.*67A>C MANE Select NP_000065.1:n.*67A>C