Canonical Allele Identifier: CA518856030

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741466A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659307A>G , CM000685.2:g.136659307A>G	GRCh38
NC_000023.10:g.135741466A>G , CM000685.1:g.135741466A>G	GRCh37
NC_000023.9:g.135569132A>G	NCBI36
NG_007280.1:g.16131A>G , LRG_141:g.16131A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*296A>G	ENSP00000512122.1:n.*296A>G
ENST00000695725.1:c.*233A>G	ENSP00000512123.1:n.*233A>G
ENST00000695726.1:n.2646A>G
ENST00000695729.1:n.3481A>G
ENST00000370629.7:c.678A>G MANE Select	ENSP00000359663.2:p.Gly226=
ENST00000370628.2:c.615A>G	ENSP00000359662.2:p.Gly205=
ENST00000370629.6:c.678A>G	ENSP00000359663.2:p.Gly226=
NM_000074.2:c.678A>G , LRG_141t1:c.678A>G	NP_000065.1:p.Gly226=
NM_000074.3:c.678A>G MANE Select	NP_000065.1:p.Gly226=