Canonical Allele Identifier: CA871912477

Gene: CD40LG

Linked Data

• dbSNP Id: rs1315652295
• gnomAD v4: X-136658914-T-C
• MyVariant Identifiers: chrX:g.135741073T>C (hg19) ; chrX:g.136658914T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136658914T>C , CM000685.2:g.136658914T>C	GRCh38
NC_000023.10:g.135741073T>C , CM000685.1:g.135741073T>C	GRCh37
NC_000023.9:g.135568739T>C	NCBI36
NG_007280.1:g.15738T>C , LRG_141:g.15738T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*28-125T>C	ENSP00000512122.1:n.*28-125T>C
ENST00000695725.1:c.157-125T>C	ENSP00000512123.1:n.157-125T>C
ENST00000695726.1:n.2378-125T>C
ENST00000695729.1:n.3213-125T>C
ENST00000370629.7:c.410-125T>C MANE Select	ENSP00000359663.2:n.410-125T>C
ENST00000370628.2:c.347-125T>C	ENSP00000359662.2:n.347-125T>C
ENST00000370629.6:c.410-125T>C	ENSP00000359663.2:n.410-125T>C
NM_000074.2:c.410-125T>C , LRG_141t1:c.410-125T>C	NP_000065.1:n.410-125T>C
NM_000074.3:c.410-125T>C MANE Select	NP_000065.1:n.410-125T>C