Canonical Allele Identifier: CA414756305
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659273C>A , CM000685.2:g.136659273C>A GRCh38
NC_000023.10:g.135741432C>A , CM000685.1:g.135741432C>A GRCh37
NC_000023.9:g.135569098C>A NCBI36
NG_007280.1:g.16097C>A , LRG_141:g.16097C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*262C>A ENSP00000512122.1:n.*262C>A
ENST00000695725.1:c.*199C>A ENSP00000512123.1:n.*199C>A
ENST00000695726.1:n.2612C>A
ENST00000695729.1:n.3447C>A
ENST00000370629.7:c.644C>A MANE Select ENSP00000359663.2:p.Ala215Asp
ENST00000370628.2:c.581C>A ENSP00000359662.2:p.Ala194Asp
ENST00000370629.6:c.644C>A ENSP00000359663.2:p.Ala215Asp
NM_000074.2:c.644C>A , LRG_141t1:c.644C>A NP_000065.1:p.Ala215Asp
NM_000074.3:c.644C>A MANE Select NP_000065.1:p.Ala215Asp