Canonical Allele Identifier: CA414751658

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135730471A>C (hg19) ; chrX:g.136648312A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648312A>C , CM000685.2:g.136648312A>C	GRCh38
NC_000023.10:g.135730471A>C , CM000685.1:g.135730471A>C	GRCh37
NC_000023.9:g.135558137A>C	NCBI36
NG_007280.1:g.5136A>C , LRG_141:g.5136A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.64A>C	ENSP00000512122.1:p.Lys22Gln
ENST00000695725.1:c.64A>C	ENSP00000512123.1:p.Lys22Gln
ENST00000695726.1:n.107A>C
ENST00000695727.1:n.51A>C
ENST00000695728.1:n.51A>C
ENST00000370629.7:c.64A>C MANE Select	ENSP00000359663.2:p.Lys22Gln
ENST00000370628.2:c.64A>C	ENSP00000359662.2:p.Lys22Gln
ENST00000370629.6:c.64A>C	ENSP00000359663.2:p.Lys22Gln
NM_000074.2:c.64A>C , LRG_141t1:c.64A>C	NP_000065.1:p.Lys22Gln
NM_000074.3:c.64A>C MANE Select	NP_000065.1:p.Lys22Gln