Canonical Allele Identifier: CA414756166

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741408G>T (hg19) ; chrX:g.136659249G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659249G>T , CM000685.2:g.136659249G>T	GRCh38
NC_000023.10:g.135741408G>T , CM000685.1:g.135741408G>T	GRCh37
NC_000023.9:g.135569074G>T	NCBI36
NG_007280.1:g.16073G>T , LRG_141:g.16073G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*238G>T	ENSP00000512122.1:n.*238G>T
ENST00000695725.1:c.*175G>T	ENSP00000512123.1:n.*175G>T
ENST00000695726.1:n.2588G>T
ENST00000695729.1:n.3423G>T
ENST00000370629.7:c.620G>T MANE Select	ENSP00000359663.2:p.Arg207Ile
ENST00000370628.2:c.557G>T	ENSP00000359662.2:p.Arg186Ile
ENST00000370629.6:c.620G>T	ENSP00000359663.2:p.Arg207Ile
NM_000074.2:c.620G>T , LRG_141t1:c.620G>T	NP_000065.1:p.Arg207Ile
NM_000074.3:c.620G>T MANE Select	NP_000065.1:p.Arg207Ile