Canonical Allele Identifier: CA414755609

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741224T>C (hg19) ; chrX:g.136659065T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659065T>C , CM000685.2:g.136659065T>C	GRCh38
NC_000023.10:g.135741224T>C , CM000685.1:g.135741224T>C	GRCh37
NC_000023.9:g.135568890T>C	NCBI36
NG_007280.1:g.15889T>C , LRG_141:g.15889T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*54T>C	ENSP00000512122.1:n.*54T>C
ENST00000695725.1:c.183T>C	ENSP00000512123.1:p.Thr61=
ENST00000695726.1:n.2404T>C
ENST00000695729.1:n.3239T>C
ENST00000370629.7:c.436T>C MANE Select	ENSP00000359663.2:p.Tyr146His
ENST00000370628.2:c.373T>C	ENSP00000359662.2:p.Tyr125His
ENST00000370629.6:c.436T>C	ENSP00000359663.2:p.Tyr146His
NM_000074.2:c.436T>C , LRG_141t1:c.436T>C	NP_000065.1:p.Tyr146His
NM_000074.3:c.436T>C MANE Select	NP_000065.1:p.Tyr146His