Canonical Allele Identifier: CA645125314

Gene: CD40LG

Linked Data

• dbSNP Id: rs1214481274
• gnomAD v2: X-135741086-G-A
• gnomAD v3: X-136658927-G-A
• gnomAD v4: X-136658927-G-A
• MyVariant Identifiers: chrX:g.135741086G>A (hg19) ; chrX:g.136658927G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136658927G>A , CM000685.2:g.136658927G>A	GRCh38
NC_000023.10:g.135741086G>A , CM000685.1:g.135741086G>A	GRCh37
NC_000023.9:g.135568752G>A	NCBI36
NG_007280.1:g.15751G>A , LRG_141:g.15751G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*28-112G>A	ENSP00000512122.1:n.*28-112G>A
ENST00000695725.1:c.157-112G>A	ENSP00000512123.1:n.157-112G>A
ENST00000695726.1:n.2378-112G>A
ENST00000695729.1:n.3213-112G>A
ENST00000370629.7:c.410-112G>A MANE Select	ENSP00000359663.2:n.410-112G>A
ENST00000370628.2:c.347-112G>A	ENSP00000359662.2:n.347-112G>A
ENST00000370629.6:c.410-112G>A	ENSP00000359663.2:n.410-112G>A
NM_000074.2:c.410-112G>A , LRG_141t1:c.410-112G>A	NP_000065.1:n.410-112G>A
NM_000074.3:c.410-112G>A MANE Select	NP_000065.1:n.410-112G>A