Canonical Allele Identifier: CA518855989
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741403A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659244A>G , CM000685.2:g.136659244A>G GRCh38
NC_000023.10:g.135741403A>G , CM000685.1:g.135741403A>G GRCh37
NC_000023.9:g.135569069A>G NCBI36
NG_007280.1:g.16068A>G , LRG_141:g.16068A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*233A>G ENSP00000512122.1:n.*233A>G
ENST00000695725.1:c.*170A>G ENSP00000512123.1:n.*170A>G
ENST00000695726.1:n.2583A>G
ENST00000695729.1:n.3418A>G
ENST00000370629.7:c.615A>G MANE Select ENSP00000359663.2:p.Leu205=
ENST00000370628.2:c.552A>G ENSP00000359662.2:p.Leu184=
ENST00000370629.6:c.615A>G ENSP00000359663.2:p.Leu205=
NM_000074.2:c.615A>G , LRG_141t1:c.615A>G NP_000065.1:p.Leu205=
NM_000074.3:c.615A>G MANE Select NP_000065.1:p.Leu205=