Canonical Allele Identifier: CA414755705

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741267A>G (hg19) ; chrX:g.136659108A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659108A>G , CM000685.2:g.136659108A>G	GRCh38
NC_000023.10:g.135741267A>G , CM000685.1:g.135741267A>G	GRCh37
NC_000023.9:g.135568933A>G	NCBI36
NG_007280.1:g.15932A>G , LRG_141:g.15932A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*97A>G	ENSP00000512122.1:n.*97A>G
ENST00000695725.1:c.*34A>G	ENSP00000512123.1:n.*34A>G
ENST00000695726.1:n.2447A>G
ENST00000695729.1:n.3282A>G
ENST00000370629.7:c.479A>G MANE Select	ENSP00000359663.2:p.Gln160Arg
ENST00000370628.2:c.416A>G	ENSP00000359662.2:p.Gln139Arg
ENST00000370629.6:c.479A>G	ENSP00000359663.2:p.Gln160Arg
NM_000074.2:c.479A>G , LRG_141t1:c.479A>G	NP_000065.1:p.Gln160Arg
NM_000074.3:c.479A>G MANE Select	NP_000065.1:p.Gln160Arg