Canonical Allele Identifier: CA414756252

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741423A>T (hg19) ; chrX:g.136659264A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659264A>T , CM000685.2:g.136659264A>T	GRCh38
NC_000023.10:g.135741423A>T , CM000685.1:g.135741423A>T	GRCh37
NC_000023.9:g.135569089A>T	NCBI36
NG_007280.1:g.16088A>T , LRG_141:g.16088A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*253A>T	ENSP00000512122.1:n.*253A>T
ENST00000695725.1:c.*190A>T	ENSP00000512123.1:n.*190A>T
ENST00000695726.1:n.2603A>T
ENST00000695729.1:n.3438A>T
ENST00000370629.7:c.635A>T MANE Select	ENSP00000359663.2:p.His212Leu
ENST00000370628.2:c.572A>T	ENSP00000359662.2:p.His191Leu
ENST00000370629.6:c.635A>T	ENSP00000359663.2:p.His212Leu
NM_000074.2:c.635A>T , LRG_141t1:c.635A>T	NP_000065.1:p.His212Leu
NM_000074.3:c.635A>T MANE Select	NP_000065.1:p.His212Leu