Canonical Allele Identifier: CA518856069

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741523C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659364C>T , CM000685.2:g.136659364C>T	GRCh38
NC_000023.10:g.135741523C>T , CM000685.1:g.135741523C>T	GRCh37
NC_000023.9:g.135569189C>T	NCBI36
NG_007280.1:g.16188C>T , LRG_141:g.16188C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*353C>T	ENSP00000512122.1:n.*353C>T
ENST00000695725.1:c.*290C>T	ENSP00000512123.1:n.*290C>T
ENST00000695726.1:n.2703C>T
ENST00000695729.1:n.3538C>T
ENST00000370629.7:c.735C>T MANE Select	ENSP00000359663.2:p.Ser245=
ENST00000370628.2:c.672C>T	ENSP00000359662.2:p.Ser224=
ENST00000370629.6:c.735C>T	ENSP00000359663.2:p.Ser245=
NM_000074.2:c.735C>T , LRG_141t1:c.735C>T	NP_000065.1:p.Ser245=
NM_000074.3:c.735C>T MANE Select	NP_000065.1:p.Ser245=