Canonical Allele Identifier: CA414755997

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659224-G-C
• MyVariant Identifiers: chrX:g.135741383G>C (hg19) ; chrX:g.136659224G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659224G>C , CM000685.2:g.136659224G>C	GRCh38
NC_000023.10:g.135741383G>C , CM000685.1:g.135741383G>C	GRCh37
NC_000023.9:g.135569049G>C	NCBI36
NG_007280.1:g.16048G>C , LRG_141:g.16048G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*213G>C	ENSP00000512122.1:n.*213G>C
ENST00000695725.1:c.*150G>C	ENSP00000512123.1:n.*150G>C
ENST00000695726.1:n.2563G>C
ENST00000695729.1:n.3398G>C
ENST00000370629.7:c.595G>C MANE Select	ENSP00000359663.2:p.Gly199Arg
ENST00000370628.2:c.532G>C	ENSP00000359662.2:p.Gly178Arg
ENST00000370629.6:c.595G>C	ENSP00000359663.2:p.Gly199Arg
NM_000074.2:c.595G>C , LRG_141t1:c.595G>C	NP_000065.1:p.Gly199Arg
NM_000074.3:c.595G>C MANE Select	NP_000065.1:p.Gly199Arg