Canonical Allele Identifier: CA414755582

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741212G>T (hg19) ; chrX:g.136659053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659053G>T , CM000685.2:g.136659053G>T	GRCh38
NC_000023.10:g.135741212G>T , CM000685.1:g.135741212G>T	GRCh37
NC_000023.9:g.135568878G>T	NCBI36
NG_007280.1:g.15877G>T , LRG_141:g.15877G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*42G>T	ENSP00000512122.1:n.*42G>T
ENST00000695725.1:c.171G>T	ENSP00000512123.1:p.Leu57=
ENST00000695726.1:n.2392G>T
ENST00000695729.1:n.3227G>T
ENST00000370629.7:c.424G>T MANE Select	ENSP00000359663.2:p.Glu142Ter
ENST00000370628.2:c.361G>T	ENSP00000359662.2:p.Glu121Ter
ENST00000370629.6:c.424G>T	ENSP00000359663.2:p.Glu142Ter
NM_000074.2:c.424G>T , LRG_141t1:c.424G>T	NP_000065.1:p.Glu142Ter
NM_000074.3:c.424G>T MANE Select	NP_000065.1:p.Glu142Ter