Canonical Allele Identifier: CA414756390

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741452T>G (hg19) ; chrX:g.136659293T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659293T>G , CM000685.2:g.136659293T>G	GRCh38
NC_000023.10:g.135741452T>G , CM000685.1:g.135741452T>G	GRCh37
NC_000023.9:g.135569118T>G	NCBI36
NG_007280.1:g.16117T>G , LRG_141:g.16117T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*282T>G	ENSP00000512122.1:n.*282T>G
ENST00000695725.1:c.*219T>G	ENSP00000512123.1:n.*219T>G
ENST00000695726.1:n.2632T>G
ENST00000695729.1:n.3467T>G
ENST00000370629.7:c.664T>G MANE Select	ENSP00000359663.2:p.Ser222Ala
ENST00000370628.2:c.601T>G	ENSP00000359662.2:p.Ser201Ala
ENST00000370629.6:c.664T>G	ENSP00000359663.2:p.Ser222Ala
NM_000074.2:c.664T>G , LRG_141t1:c.664T>G	NP_000065.1:p.Ser222Ala
NM_000074.3:c.664T>G MANE Select	NP_000065.1:p.Ser222Ala