Canonical Allele Identifier: CA518856033

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741469A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659310A>T , CM000685.2:g.136659310A>T	GRCh38
NC_000023.10:g.135741469A>T , CM000685.1:g.135741469A>T	GRCh37
NC_000023.9:g.135569135A>T	NCBI36
NG_007280.1:g.16134A>T , LRG_141:g.16134A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*299A>T	ENSP00000512122.1:n.*299A>T
ENST00000695725.1:c.*236A>T	ENSP00000512123.1:n.*236A>T
ENST00000695726.1:n.2649A>T
ENST00000695729.1:n.3484A>T
ENST00000370629.7:c.681A>T MANE Select	ENSP00000359663.2:p.Gly227=
ENST00000370628.2:c.618A>T	ENSP00000359662.2:p.Gly206=
ENST00000370629.6:c.681A>T	ENSP00000359663.2:p.Gly227=
NM_000074.2:c.681A>T , LRG_141t1:c.681A>T	NP_000065.1:p.Gly227=
NM_000074.3:c.681A>T MANE Select	NP_000065.1:p.Gly227=