Canonical Allele Identifier: CA2694817229

Gene: CD40LG

Linked Data

• gnomAD v4: X-136648425-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648425T>G , CM000685.2:g.136648425T>G	GRCh38
NC_000023.10:g.135730584T>G , CM000685.1:g.135730584T>G	GRCh37
NC_000023.9:g.135558250T>G	NCBI36
NG_007280.1:g.5249T>G , LRG_141:g.5249T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.156+21T>G	ENSP00000512122.1:n.156+21T>G
ENST00000695725.1:c.156+21T>G	ENSP00000512123.1:n.156+21T>G
ENST00000695726.1:n.199+21T>G
ENST00000695727.1:n.143+21T>G
ENST00000695728.1:n.143+21T>G
ENST00000370629.7:c.156+21T>G MANE Select	ENSP00000359663.2:n.156+21T>G
ENST00000370628.2:c.156+21T>G	ENSP00000359662.2:n.156+21T>G
ENST00000370629.6:c.156+21T>G	ENSP00000359663.2:n.156+21T>G
NM_000074.2:c.156+21T>G , LRG_141t1:c.156+21T>G	NP_000065.1:n.156+21T>G
NM_000074.3:c.156+21T>G MANE Select	NP_000065.1:n.156+21T>G