Canonical Allele Identifier: CA414755566

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741205G>C (hg19) ; chrX:g.136659046G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659046G>C , CM000685.2:g.136659046G>C	GRCh38
NC_000023.10:g.135741205G>C , CM000685.1:g.135741205G>C	GRCh37
NC_000023.9:g.135568871G>C	NCBI36
NG_007280.1:g.15870G>C , LRG_141:g.15870G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*35G>C	ENSP00000512122.1:n.*35G>C
ENST00000695725.1:c.164G>C	ENSP00000512123.1:p.Ser55Thr
ENST00000695726.1:n.2385G>C
ENST00000695729.1:n.3220G>C
ENST00000370629.7:c.417G>C MANE Select	ENSP00000359663.2:p.Gln139His
ENST00000370628.2:c.354G>C	ENSP00000359662.2:p.Gln118His
ENST00000370629.6:c.417G>C	ENSP00000359663.2:p.Gln139His
NM_000074.2:c.417G>C , LRG_141t1:c.417G>C	NP_000065.1:p.Gln139His
NM_000074.3:c.417G>C MANE Select	NP_000065.1:p.Gln139His