Canonical Allele Identifier: CA518856068

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741520A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659361A>T , CM000685.2:g.136659361A>T	GRCh38
NC_000023.10:g.135741520A>T , CM000685.1:g.135741520A>T	GRCh37
NC_000023.9:g.135569186A>T	NCBI36
NG_007280.1:g.16185A>T , LRG_141:g.16185A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*350A>T	ENSP00000512122.1:n.*350A>T
ENST00000695725.1:c.*287A>T	ENSP00000512123.1:n.*287A>T
ENST00000695726.1:n.2700A>T
ENST00000695729.1:n.3535A>T
ENST00000370629.7:c.732A>T MANE Select	ENSP00000359663.2:p.Pro244=
ENST00000370628.2:c.669A>T	ENSP00000359662.2:p.Pro223=
ENST00000370629.6:c.732A>T	ENSP00000359663.2:p.Pro244=
NM_000074.2:c.732A>T , LRG_141t1:c.732A>T	NP_000065.1:p.Pro244=
NM_000074.3:c.732A>T MANE Select	NP_000065.1:p.Pro244=