Canonical Allele Identifier: CA414751553

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135730450A>C (hg19) ; chrX:g.136648291A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648291A>C , CM000685.2:g.136648291A>C	GRCh38
NC_000023.10:g.135730450A>C , CM000685.1:g.135730450A>C	GRCh37
NC_000023.9:g.135558116A>C	NCBI36
NG_007280.1:g.5115A>C , LRG_141:g.5115A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.43A>C	ENSP00000512122.1:p.Thr15Pro
ENST00000695725.1:c.43A>C	ENSP00000512123.1:p.Thr15Pro
ENST00000695726.1:n.86A>C
ENST00000695727.1:n.30A>C
ENST00000695728.1:n.30A>C
ENST00000370629.7:c.43A>C MANE Select	ENSP00000359663.2:p.Thr15Pro
ENST00000370628.2:c.43A>C	ENSP00000359662.2:p.Thr15Pro
ENST00000370629.6:c.43A>C	ENSP00000359663.2:p.Thr15Pro
NM_000074.2:c.43A>C , LRG_141t1:c.43A>C	NP_000065.1:p.Thr15Pro
NM_000074.3:c.43A>C MANE Select	NP_000065.1:p.Thr15Pro