Canonical Allele Identifier: CA414756778

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659348-A-G
• MyVariant Identifiers: chrX:g.135741507A>G (hg19) ; chrX:g.136659348A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659348A>G , CM000685.2:g.136659348A>G	GRCh38
NC_000023.10:g.135741507A>G , CM000685.1:g.135741507A>G	GRCh37
NC_000023.9:g.135569173A>G	NCBI36
NG_007280.1:g.16172A>G , LRG_141:g.16172A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*337A>G	ENSP00000512122.1:n.*337A>G
ENST00000695725.1:c.*274A>G	ENSP00000512123.1:n.*274A>G
ENST00000695726.1:n.2687A>G
ENST00000695729.1:n.3522A>G
ENST00000370629.7:c.719A>G MANE Select	ENSP00000359663.2:p.Asn240Ser
ENST00000370628.2:c.656A>G	ENSP00000359662.2:p.Asn219Ser
ENST00000370629.6:c.719A>G	ENSP00000359663.2:p.Asn240Ser
NM_000074.2:c.719A>G , LRG_141t1:c.719A>G	NP_000065.1:p.Asn240Ser
NM_000074.3:c.719A>G MANE Select	NP_000065.1:p.Asn240Ser