Canonical Allele Identifier: CA414757082

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741548A>C (hg19) ; chrX:g.136659389A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659389A>C , CM000685.2:g.136659389A>C	GRCh38
NC_000023.10:g.135741548A>C , CM000685.1:g.135741548A>C	GRCh37
NC_000023.9:g.135569214A>C	NCBI36
NG_007280.1:g.16213A>C , LRG_141:g.16213A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*378A>C	ENSP00000512122.1:n.*378A>C
ENST00000695725.1:c.*315A>C	ENSP00000512123.1:n.*315A>C
ENST00000695726.1:n.2728A>C
ENST00000695729.1:n.3563A>C
ENST00000370629.7:c.760A>C MANE Select	ENSP00000359663.2:p.Thr254Pro
ENST00000370628.2:c.697A>C	ENSP00000359662.2:p.Thr233Pro
ENST00000370629.6:c.760A>C	ENSP00000359663.2:p.Thr254Pro
NM_000074.2:c.760A>C , LRG_141t1:c.760A>C	NP_000065.1:p.Thr254Pro
NM_000074.3:c.760A>C MANE Select	NP_000065.1:p.Thr254Pro