Canonical Allele Identifier: CA414756316

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741436A>T (hg19) ; chrX:g.136659277A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659277A>T , CM000685.2:g.136659277A>T	GRCh38
NC_000023.10:g.135741436A>T , CM000685.1:g.135741436A>T	GRCh37
NC_000023.9:g.135569102A>T	NCBI36
NG_007280.1:g.16101A>T , LRG_141:g.16101A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*266A>T	ENSP00000512122.1:n.*266A>T
ENST00000695725.1:c.*203A>T	ENSP00000512123.1:n.*203A>T
ENST00000695726.1:n.2616A>T
ENST00000695729.1:n.3451A>T
ENST00000370629.7:c.648A>T MANE Select	ENSP00000359663.2:p.Lys216Asn
ENST00000370628.2:c.585A>T	ENSP00000359662.2:p.Lys195Asn
ENST00000370629.6:c.648A>T	ENSP00000359663.2:p.Lys216Asn
NM_000074.2:c.648A>T , LRG_141t1:c.648A>T	NP_000065.1:p.Lys216Asn
NM_000074.3:c.648A>T MANE Select	NP_000065.1:p.Lys216Asn