Canonical Allele Identifier: CA414756225

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741419A>T (hg19) ; chrX:g.136659260A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659260A>T , CM000685.2:g.136659260A>T	GRCh38
NC_000023.10:g.135741419A>T , CM000685.1:g.135741419A>T	GRCh37
NC_000023.9:g.135569085A>T	NCBI36
NG_007280.1:g.16084A>T , LRG_141:g.16084A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*249A>T	ENSP00000512122.1:n.*249A>T
ENST00000695725.1:c.*186A>T	ENSP00000512123.1:n.*186A>T
ENST00000695726.1:n.2599A>T
ENST00000695729.1:n.3434A>T
ENST00000370629.7:c.631A>T MANE Select	ENSP00000359663.2:p.Thr211Ser
ENST00000370628.2:c.568A>T	ENSP00000359662.2:p.Thr190Ser
ENST00000370629.6:c.631A>T	ENSP00000359663.2:p.Thr211Ser
NM_000074.2:c.631A>T , LRG_141t1:c.631A>T	NP_000065.1:p.Thr211Ser
NM_000074.3:c.631A>T MANE Select	NP_000065.1:p.Thr211Ser