Canonical Allele Identifier: CA414756528

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741474T>G (hg19) ; chrX:g.136659315T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659315T>G , CM000685.2:g.136659315T>G	GRCh38
NC_000023.10:g.135741474T>G , CM000685.1:g.135741474T>G	GRCh37
NC_000023.9:g.135569140T>G	NCBI36
NG_007280.1:g.16139T>G , LRG_141:g.16139T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*304T>G	ENSP00000512122.1:n.*304T>G
ENST00000695725.1:c.*241T>G	ENSP00000512123.1:n.*241T>G
ENST00000695726.1:n.2654T>G
ENST00000695729.1:n.3489T>G
ENST00000370629.7:c.686T>G MANE Select	ENSP00000359663.2:p.Phe229Cys
ENST00000370628.2:c.623T>G	ENSP00000359662.2:p.Phe208Cys
ENST00000370629.6:c.686T>G	ENSP00000359663.2:p.Phe229Cys
NM_000074.2:c.686T>G , LRG_141t1:c.686T>G	NP_000065.1:p.Phe229Cys
NM_000074.3:c.686T>G MANE Select	NP_000065.1:p.Phe229Cys