Canonical Allele Identifier: CA414756958

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741532C>A (hg19) ; chrX:g.136659373C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659373C>A , CM000685.2:g.136659373C>A	GRCh38
NC_000023.10:g.135741532C>A , CM000685.1:g.135741532C>A	GRCh37
NC_000023.9:g.135569198C>A	NCBI36
NG_007280.1:g.16197C>A , LRG_141:g.16197C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*362C>A	ENSP00000512122.1:n.*362C>A
ENST00000695725.1:c.*299C>A	ENSP00000512123.1:n.*299C>A
ENST00000695726.1:n.2712C>A
ENST00000695729.1:n.3547C>A
ENST00000370629.7:c.744C>A MANE Select	ENSP00000359663.2:p.Ser248Arg
ENST00000370628.2:c.681C>A	ENSP00000359662.2:p.Ser227Arg
ENST00000370629.6:c.744C>A	ENSP00000359663.2:p.Ser248Arg
NM_000074.2:c.744C>A , LRG_141t1:c.744C>A	NP_000065.1:p.Ser248Arg
NM_000074.3:c.744C>A MANE Select	NP_000065.1:p.Ser248Arg