Canonical Allele Identifier: CA414756490

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659311-G-A
• MyVariant Identifiers: chrX:g.135741470G>A (hg19) ; chrX:g.136659311G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659311G>A , CM000685.2:g.136659311G>A	GRCh38
NC_000023.10:g.135741470G>A , CM000685.1:g.135741470G>A	GRCh37
NC_000023.9:g.135569136G>A	NCBI36
NG_007280.1:g.16135G>A , LRG_141:g.16135G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*300G>A	ENSP00000512122.1:n.*300G>A
ENST00000695725.1:c.*237G>A	ENSP00000512123.1:n.*237G>A
ENST00000695726.1:n.2650G>A
ENST00000695729.1:n.3485G>A
ENST00000370629.7:c.682G>A MANE Select	ENSP00000359663.2:p.Val228Ile
ENST00000370628.2:c.619G>A	ENSP00000359662.2:p.Val207Ile
ENST00000370629.6:c.682G>A	ENSP00000359663.2:p.Val228Ile
NM_000074.2:c.682G>A , LRG_141t1:c.682G>A	NP_000065.1:p.Val228Ile
NM_000074.3:c.682G>A MANE Select	NP_000065.1:p.Val228Ile