Canonical Allele Identifier: CA2694818742

Gene: CD40LG

Linked Data

• gnomAD v4: X-136658937-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136658937C>G , CM000685.2:g.136658937C>G	GRCh38
NC_000023.10:g.135741096C>G , CM000685.1:g.135741096C>G	GRCh37
NC_000023.9:g.135568762C>G	NCBI36
NG_007280.1:g.15761C>G , LRG_141:g.15761C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*28-102C>G	ENSP00000512122.1:n.*28-102C>G
ENST00000695725.1:c.157-102C>G	ENSP00000512123.1:n.157-102C>G
ENST00000695726.1:n.2378-102C>G
ENST00000695729.1:n.3213-102C>G
ENST00000370629.7:c.410-102C>G MANE Select	ENSP00000359663.2:n.410-102C>G
ENST00000370628.2:c.347-102C>G	ENSP00000359662.2:n.347-102C>G
ENST00000370629.6:c.410-102C>G	ENSP00000359663.2:n.410-102C>G
NM_000074.2:c.410-102C>G , LRG_141t1:c.410-102C>G	NP_000065.1:n.410-102C>G
NM_000074.3:c.410-102C>G MANE Select	NP_000065.1:n.410-102C>G