Canonical Allele Identifier: CA518779147

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135730494T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648335T>C , CM000685.2:g.136648335T>C	GRCh38
NC_000023.10:g.135730494T>C , CM000685.1:g.135730494T>C	GRCh37
NC_000023.9:g.135558160T>C	NCBI36
NG_007280.1:g.5159T>C , LRG_141:g.5159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.87T>C	ENSP00000512122.1:p.Thr29=
ENST00000695725.1:c.87T>C	ENSP00000512123.1:p.Thr29=
ENST00000695726.1:n.130T>C
ENST00000695727.1:n.74T>C
ENST00000695728.1:n.74T>C
ENST00000370629.7:c.87T>C MANE Select	ENSP00000359663.2:p.Thr29=
ENST00000370628.2:c.87T>C	ENSP00000359662.2:p.Thr29=
ENST00000370629.6:c.87T>C	ENSP00000359663.2:p.Thr29=
NM_000074.2:c.87T>C , LRG_141t1:c.87T>C	NP_000065.1:p.Thr29=
NM_000074.3:c.87T>C MANE Select	NP_000065.1:p.Thr29=