Canonical Allele Identifier: CA518856020
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741451A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659292A>G , CM000685.2:g.136659292A>G GRCh38
NC_000023.10:g.135741451A>G , CM000685.1:g.135741451A>G GRCh37
NC_000023.9:g.135569117A>G NCBI36
NG_007280.1:g.16116A>G , LRG_141:g.16116A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*281A>G ENSP00000512122.1:n.*281A>G
ENST00000695725.1:c.*218A>G ENSP00000512123.1:n.*218A>G
ENST00000695726.1:n.2631A>G
ENST00000695729.1:n.3466A>G
ENST00000370629.7:c.663A>G MANE Select ENSP00000359663.2:p.Gln221=
ENST00000370628.2:c.600A>G ENSP00000359662.2:p.Gln200=
ENST00000370629.6:c.663A>G ENSP00000359663.2:p.Gln221=
NM_000074.2:c.663A>G , LRG_141t1:c.663A>G NP_000065.1:p.Gln221=
NM_000074.3:c.663A>G MANE Select NP_000065.1:p.Gln221=