Canonical Allele Identifier: CA414755564

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741204A>C (hg19) ; chrX:g.136659045A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659045A>C , CM000685.2:g.136659045A>C	GRCh38
NC_000023.10:g.135741204A>C , CM000685.1:g.135741204A>C	GRCh37
NC_000023.9:g.135568870A>C	NCBI36
NG_007280.1:g.15869A>C , LRG_141:g.15869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*34A>C	ENSP00000512122.1:n.*34A>C
ENST00000695725.1:c.163A>C	ENSP00000512123.1:p.Ser55Arg
ENST00000695726.1:n.2384A>C
ENST00000695729.1:n.3219A>C
ENST00000370629.7:c.416A>C MANE Select	ENSP00000359663.2:p.Gln139Pro
ENST00000370628.2:c.353A>C	ENSP00000359662.2:p.Gln118Pro
ENST00000370629.6:c.416A>C	ENSP00000359663.2:p.Gln139Pro
NM_000074.2:c.416A>C , LRG_141t1:c.416A>C	NP_000065.1:p.Gln139Pro
NM_000074.3:c.416A>C MANE Select	NP_000065.1:p.Gln139Pro