Canonical Allele Identifier: CA414755578

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741210C>G (hg19) ; chrX:g.136659051C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659051C>G , CM000685.2:g.136659051C>G	GRCh38
NC_000023.10:g.135741210C>G , CM000685.1:g.135741210C>G	GRCh37
NC_000023.9:g.135568876C>G	NCBI36
NG_007280.1:g.15875C>G , LRG_141:g.15875C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*40C>G	ENSP00000512122.1:n.*40C>G
ENST00000695725.1:c.169C>G	ENSP00000512123.1:p.Leu57Val
ENST00000695726.1:n.2390C>G
ENST00000695729.1:n.3225C>G
ENST00000370629.7:c.422C>G MANE Select	ENSP00000359663.2:p.Ala141Gly
ENST00000370628.2:c.359C>G	ENSP00000359662.2:p.Ala120Gly
ENST00000370629.6:c.422C>G	ENSP00000359663.2:p.Ala141Gly
NM_000074.2:c.422C>G , LRG_141t1:c.422C>G	NP_000065.1:p.Ala141Gly
NM_000074.3:c.422C>G MANE Select	NP_000065.1:p.Ala141Gly