Canonical Allele Identifier: CA414757238

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741572T>C (hg19) ; chrX:g.136659413T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659413T>C , CM000685.2:g.136659413T>C	GRCh38
NC_000023.10:g.135741572T>C , CM000685.1:g.135741572T>C	GRCh37
NC_000023.9:g.135569238T>C	NCBI36
NG_007280.1:g.16237T>C , LRG_141:g.16237T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*402T>C	ENSP00000512122.1:n.*402T>C
ENST00000695725.1:c.*339T>C	ENSP00000512123.1:n.*339T>C
ENST00000695726.1:n.2752T>C
ENST00000695729.1:n.3587T>C
ENST00000370629.7:c.784T>C MANE Select	ENSP00000359663.2:p.Ter262Arg
ENST00000370628.2:c.721T>C	ENSP00000359662.2:p.Ter241Arg
ENST00000370629.6:c.784T>C	ENSP00000359663.2:p.Ter262Arg
NM_000074.2:c.784T>C , LRG_141t1:c.784T>C	NP_000065.1:p.Ter262Arg
NM_000074.3:c.784T>C MANE Select	NP_000065.1:p.Ter262Arg