Canonical Allele Identifier: CA414751494

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135730436C>T (hg19) ; chrX:g.136648277C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648277C>T , CM000685.2:g.136648277C>T	GRCh38
NC_000023.10:g.135730436C>T , CM000685.1:g.135730436C>T	GRCh37
NC_000023.9:g.135558102C>T	NCBI36
NG_007280.1:g.5101C>T , LRG_141:g.5101C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.29C>T	ENSP00000512122.1:p.Pro10Leu
ENST00000695725.1:c.29C>T	ENSP00000512123.1:p.Pro10Leu
ENST00000695726.1:n.72C>T
ENST00000695727.1:n.16C>T
ENST00000695728.1:n.16C>T
ENST00000370629.7:c.29C>T MANE Select	ENSP00000359663.2:p.Pro10Leu
ENST00000370628.2:c.29C>T	ENSP00000359662.2:p.Pro10Leu
ENST00000370629.6:c.29C>T	ENSP00000359663.2:p.Pro10Leu
NM_000074.2:c.29C>T , LRG_141t1:c.29C>T	NP_000065.1:p.Pro10Leu
NM_000074.3:c.29C>T MANE Select	NP_000065.1:p.Pro10Leu