Canonical Allele Identifier: CA414755833

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659165-C-A
• MyVariant Identifiers: chrX:g.135741324C>A (hg19) ; chrX:g.136659165C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659165C>A , CM000685.2:g.136659165C>A	GRCh38
NC_000023.10:g.135741324C>A , CM000685.1:g.135741324C>A	GRCh37
NC_000023.9:g.135568990C>A	NCBI36
NG_007280.1:g.15989C>A , LRG_141:g.15989C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*154C>A	ENSP00000512122.1:n.*154C>A
ENST00000695725.1:c.*91C>A	ENSP00000512123.1:n.*91C>A
ENST00000695726.1:n.2504C>A
ENST00000695729.1:n.3339C>A
ENST00000370629.7:c.536C>A MANE Select	ENSP00000359663.2:p.Ser179Tyr
ENST00000370628.2:c.473C>A	ENSP00000359662.2:p.Ser158Tyr
ENST00000370629.6:c.536C>A	ENSP00000359663.2:p.Ser179Tyr
NM_000074.2:c.536C>A , LRG_141t1:c.536C>A	NP_000065.1:p.Ser179Tyr
NM_000074.3:c.536C>A MANE Select	NP_000065.1:p.Ser179Tyr