Canonical Allele Identifier: CA2694819086

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659456-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659456A>G , CM000685.2:g.136659456A>G	GRCh38
NC_000023.10:g.135741615A>G , CM000685.1:g.135741615A>G	GRCh37
NC_000023.9:g.135569281A>G	NCBI36
NG_007280.1:g.16280A>G , LRG_141:g.16280A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*445A>G	ENSP00000512122.1:n.*445A>G
ENST00000695725.1:c.*382A>G	ENSP00000512123.1:n.*382A>G
ENST00000695726.1:n.2795A>G
ENST00000695729.1:n.3630A>G
ENST00000370629.7:c.*41A>G MANE Select	ENSP00000359663.2:n.*41A>G
ENST00000370628.2:c.*41A>G	ENSP00000359662.2:n.*41A>G
ENST00000370629.6:c.*41A>G	ENSP00000359663.2:n.*41A>G
NM_000074.2:c.*41A>G , LRG_141t1:c.*41A>G	NP_000065.1:n.*41A>G
NM_000074.3:c.*41A>G MANE Select	NP_000065.1:n.*41A>G