Canonical Allele Identifier: CA414756851

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741516A>G (hg19) ; chrX:g.136659357A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659357A>G , CM000685.2:g.136659357A>G	GRCh38
NC_000023.10:g.135741516A>G , CM000685.1:g.135741516A>G	GRCh37
NC_000023.9:g.135569182A>G	NCBI36
NG_007280.1:g.16181A>G , LRG_141:g.16181A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*346A>G	ENSP00000512122.1:n.*346A>G
ENST00000695725.1:c.*283A>G	ENSP00000512123.1:n.*283A>G
ENST00000695726.1:n.2696A>G
ENST00000695729.1:n.3531A>G
ENST00000370629.7:c.728A>G MANE Select	ENSP00000359663.2:p.Asp243Gly
ENST00000370628.2:c.665A>G	ENSP00000359662.2:p.Asp222Gly
ENST00000370629.6:c.728A>G	ENSP00000359663.2:p.Asp243Gly
NM_000074.2:c.728A>G , LRG_141t1:c.728A>G	NP_000065.1:p.Asp243Gly
NM_000074.3:c.728A>G MANE Select	NP_000065.1:p.Asp243Gly