Canonical Allele Identifier: CA414756312

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741435A>C (hg19) ; chrX:g.136659276A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659276A>C , CM000685.2:g.136659276A>C	GRCh38
NC_000023.10:g.135741435A>C , CM000685.1:g.135741435A>C	GRCh37
NC_000023.9:g.135569101A>C	NCBI36
NG_007280.1:g.16100A>C , LRG_141:g.16100A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*265A>C	ENSP00000512122.1:n.*265A>C
ENST00000695725.1:c.*202A>C	ENSP00000512123.1:n.*202A>C
ENST00000695726.1:n.2615A>C
ENST00000695729.1:n.3450A>C
ENST00000370629.7:c.647A>C MANE Select	ENSP00000359663.2:p.Lys216Thr
ENST00000370628.2:c.584A>C	ENSP00000359662.2:p.Lys195Thr
ENST00000370629.6:c.647A>C	ENSP00000359663.2:p.Lys216Thr
NM_000074.2:c.647A>C , LRG_141t1:c.647A>C	NP_000065.1:p.Lys216Thr
NM_000074.3:c.647A>C MANE Select	NP_000065.1:p.Lys216Thr