Canonical Allele Identifier: CA414756895

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741522G>C (hg19) ; chrX:g.136659363G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659363G>C , CM000685.2:g.136659363G>C	GRCh38
NC_000023.10:g.135741522G>C , CM000685.1:g.135741522G>C	GRCh37
NC_000023.9:g.135569188G>C	NCBI36
NG_007280.1:g.16187G>C , LRG_141:g.16187G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*352G>C	ENSP00000512122.1:n.*352G>C
ENST00000695725.1:c.*289G>C	ENSP00000512123.1:n.*289G>C
ENST00000695726.1:n.2702G>C
ENST00000695729.1:n.3537G>C
ENST00000370629.7:c.734G>C MANE Select	ENSP00000359663.2:p.Ser245Thr
ENST00000370628.2:c.671G>C	ENSP00000359662.2:p.Ser224Thr
ENST00000370629.6:c.734G>C	ENSP00000359663.2:p.Ser245Thr
NM_000074.2:c.734G>C , LRG_141t1:c.734G>C	NP_000065.1:p.Ser245Thr
NM_000074.3:c.734G>C MANE Select	NP_000065.1:p.Ser245Thr