Canonical Allele Identifier: CA518856040
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741487A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659328A>C , CM000685.2:g.136659328A>C GRCh38
NC_000023.10:g.135741487A>C , CM000685.1:g.135741487A>C GRCh37
NC_000023.9:g.135569153A>C NCBI36
NG_007280.1:g.16152A>C , LRG_141:g.16152A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*317A>C ENSP00000512122.1:n.*317A>C
ENST00000695725.1:c.*254A>C ENSP00000512123.1:n.*254A>C
ENST00000695726.1:n.2667A>C
ENST00000695729.1:n.3502A>C
ENST00000370629.7:c.699A>C MANE Select ENSP00000359663.2:p.Pro233=
ENST00000370628.2:c.636A>C ENSP00000359662.2:p.Pro212=
ENST00000370629.6:c.699A>C ENSP00000359663.2:p.Pro233=
NM_000074.2:c.699A>C , LRG_141t1:c.699A>C NP_000065.1:p.Pro233=
NM_000074.3:c.699A>C MANE Select NP_000065.1:p.Pro233=