Canonical Allele Identifier: CA414756852

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741516A>T (hg19) ; chrX:g.136659357A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659357A>T , CM000685.2:g.136659357A>T	GRCh38
NC_000023.10:g.135741516A>T , CM000685.1:g.135741516A>T	GRCh37
NC_000023.9:g.135569182A>T	NCBI36
NG_007280.1:g.16181A>T , LRG_141:g.16181A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*346A>T	ENSP00000512122.1:n.*346A>T
ENST00000695725.1:c.*283A>T	ENSP00000512123.1:n.*283A>T
ENST00000695726.1:n.2696A>T
ENST00000695729.1:n.3531A>T
ENST00000370629.7:c.728A>T MANE Select	ENSP00000359663.2:p.Asp243Val
ENST00000370628.2:c.665A>T	ENSP00000359662.2:p.Asp222Val
ENST00000370629.6:c.728A>T	ENSP00000359663.2:p.Asp243Val
NM_000074.2:c.728A>T , LRG_141t1:c.728A>T	NP_000065.1:p.Asp243Val
NM_000074.3:c.728A>T MANE Select	NP_000065.1:p.Asp243Val