Canonical Allele Identifier: CA414757106

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741551T>G (hg19) ; chrX:g.136659392T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659392T>G , CM000685.2:g.136659392T>G	GRCh38
NC_000023.10:g.135741551T>G , CM000685.1:g.135741551T>G	GRCh37
NC_000023.9:g.135569217T>G	NCBI36
NG_007280.1:g.16216T>G , LRG_141:g.16216T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*381T>G	ENSP00000512122.1:n.*381T>G
ENST00000695725.1:c.*318T>G	ENSP00000512123.1:n.*318T>G
ENST00000695726.1:n.2731T>G
ENST00000695729.1:n.3566T>G
ENST00000370629.7:c.763T>G MANE Select	ENSP00000359663.2:p.Ser255Ala
ENST00000370628.2:c.700T>G	ENSP00000359662.2:p.Ser234Ala
ENST00000370629.6:c.763T>G	ENSP00000359663.2:p.Ser255Ala
NM_000074.2:c.763T>G , LRG_141t1:c.763T>G	NP_000065.1:p.Ser255Ala
NM_000074.3:c.763T>G MANE Select	NP_000065.1:p.Ser255Ala