Canonical Allele Identifier: CA414755888

Gene: CD40LG

Linked Data

• dbSNP Id: rs1245452261
• gnomAD v4: X-136659191-C-T
• MyVariant Identifiers: chrX:g.135741350C>T (hg19) ; chrX:g.136659191C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659191C>T , CM000685.2:g.136659191C>T	GRCh38
NC_000023.10:g.135741350C>T , CM000685.1:g.135741350C>T	GRCh37
NC_000023.9:g.135569016C>T	NCBI36
NG_007280.1:g.16015C>T , LRG_141:g.16015C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*180C>T	ENSP00000512122.1:n.*180C>T
ENST00000695725.1:c.*117C>T	ENSP00000512123.1:n.*117C>T
ENST00000695726.1:n.2530C>T
ENST00000695729.1:n.3365C>T
ENST00000370629.7:c.562C>T MANE Select	ENSP00000359663.2:p.Pro188Ser
ENST00000370628.2:c.499C>T	ENSP00000359662.2:p.Pro167Ser
ENST00000370629.6:c.562C>T	ENSP00000359663.2:p.Pro188Ser
NM_000074.2:c.562C>T , LRG_141t1:c.562C>T	NP_000065.1:p.Pro188Ser
NM_000074.3:c.562C>T MANE Select	NP_000065.1:p.Pro188Ser