Canonical Allele Identifier: CA518855957

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741352A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659193A>T , CM000685.2:g.136659193A>T	GRCh38
NC_000023.10:g.135741352A>T , CM000685.1:g.135741352A>T	GRCh37
NC_000023.9:g.135569018A>T	NCBI36
NG_007280.1:g.16017A>T , LRG_141:g.16017A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*182A>T	ENSP00000512122.1:n.*182A>T
ENST00000695725.1:c.*119A>T	ENSP00000512123.1:n.*119A>T
ENST00000695726.1:n.2532A>T
ENST00000695729.1:n.3367A>T
ENST00000370629.7:c.564A>T MANE Select	ENSP00000359663.2:p.Pro188=
ENST00000370628.2:c.501A>T	ENSP00000359662.2:p.Pro167=
ENST00000370629.6:c.564A>T	ENSP00000359663.2:p.Pro188=
NM_000074.2:c.564A>T , LRG_141t1:c.564A>T	NP_000065.1:p.Pro188=
NM_000074.3:c.564A>T MANE Select	NP_000065.1:p.Pro188=