Canonical Allele Identifier: CA414755601
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 1005819
ClinVar RCV Id: RCV001302763
dbSNP Id: rs762639528

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659062T>A , CM000685.2:g.136659062T>A GRCh38
NC_000023.10:g.135741221T>A , CM000685.1:g.135741221T>A GRCh37
NC_000023.9:g.135568887T>A NCBI36
NG_007280.1:g.15886T>A , LRG_141:g.15886T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*51T>A ENSP00000512122.1:n.*51T>A
ENST00000695725.1:c.180T>A ENSP00000512123.1:p.Asp60Glu
ENST00000695726.1:n.2401T>A
ENST00000695729.1:n.3236T>A
ENST00000370629.7:c.433T>A MANE Select ENSP00000359663.2:p.Tyr145Asn
ENST00000370628.2:c.370T>A ENSP00000359662.2:p.Tyr124Asn
ENST00000370629.6:c.433T>A ENSP00000359663.2:p.Tyr145Asn
NM_000074.2:c.433T>A , LRG_141t1:c.433T>A NP_000065.1:p.Tyr145Asn
NM_000074.3:c.433T>A MANE Select NP_000065.1:p.Tyr145Asn