Canonical Allele Identifier: CA518856017

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741445G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659286G>C , CM000685.2:g.136659286G>C	GRCh38
NC_000023.10:g.135741445G>C , CM000685.1:g.135741445G>C	GRCh37
NC_000023.9:g.135569111G>C	NCBI36
NG_007280.1:g.16110G>C , LRG_141:g.16110G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*275G>C	ENSP00000512122.1:n.*275G>C
ENST00000695725.1:c.*212G>C	ENSP00000512123.1:n.*212G>C
ENST00000695726.1:n.2625G>C
ENST00000695729.1:n.3460G>C
ENST00000370629.7:c.657G>C MANE Select	ENSP00000359663.2:p.Gly219=
ENST00000370628.2:c.594G>C	ENSP00000359662.2:p.Gly198=
ENST00000370629.6:c.657G>C	ENSP00000359663.2:p.Gly219=
NM_000074.2:c.657G>C , LRG_141t1:c.657G>C	NP_000065.1:p.Gly219=
NM_000074.3:c.657G>C MANE Select	NP_000065.1:p.Gly219=