Canonical Allele Identifier: CA414756653

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741489G>A (hg19) ; chrX:g.136659330G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659330G>A , CM000685.2:g.136659330G>A	GRCh38
NC_000023.10:g.135741489G>A , CM000685.1:g.135741489G>A	GRCh37
NC_000023.9:g.135569155G>A	NCBI36
NG_007280.1:g.16154G>A , LRG_141:g.16154G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*319G>A	ENSP00000512122.1:n.*319G>A
ENST00000695725.1:c.*256G>A	ENSP00000512123.1:n.*256G>A
ENST00000695726.1:n.2669G>A
ENST00000695729.1:n.3504G>A
ENST00000370629.7:c.701G>A MANE Select	ENSP00000359663.2:p.Gly234Asp
ENST00000370628.2:c.638G>A	ENSP00000359662.2:p.Gly213Asp
ENST00000370629.6:c.701G>A	ENSP00000359663.2:p.Gly234Asp
NM_000074.2:c.701G>A , LRG_141t1:c.701G>A	NP_000065.1:p.Gly234Asp
NM_000074.3:c.701G>A MANE Select	NP_000065.1:p.Gly234Asp