Canonical Allele Identifier: CA871912475

Gene: CD40LG

Linked Data

• dbSNP Id: rs1400061286
• gnomAD v4: X-136658910-C-T
• MyVariant Identifiers: chrX:g.135741069C>T (hg19) ; chrX:g.136658910C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136658910C>T , CM000685.2:g.136658910C>T	GRCh38
NC_000023.10:g.135741069C>T , CM000685.1:g.135741069C>T	GRCh37
NC_000023.9:g.135568735C>T	NCBI36
NG_007280.1:g.15734C>T , LRG_141:g.15734C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*28-129C>T	ENSP00000512122.1:n.*28-129C>T
ENST00000695725.1:c.157-129C>T	ENSP00000512123.1:n.157-129C>T
ENST00000695726.1:n.2378-129C>T
ENST00000695729.1:n.3213-129C>T
ENST00000370629.7:c.410-129C>T MANE Select	ENSP00000359663.2:n.410-129C>T
ENST00000370628.2:c.347-129C>T	ENSP00000359662.2:n.347-129C>T
ENST00000370629.6:c.410-129C>T	ENSP00000359663.2:n.410-129C>T
NM_000074.2:c.410-129C>T , LRG_141t1:c.410-129C>T	NP_000065.1:n.410-129C>T
NM_000074.3:c.410-129C>T MANE Select	NP_000065.1:n.410-129C>T