Canonical Allele Identifier: CA414756073
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659235G>T , CM000685.2:g.136659235G>T GRCh38
NC_000023.10:g.135741394G>T , CM000685.1:g.135741394G>T GRCh37
NC_000023.9:g.135569060G>T NCBI36
NG_007280.1:g.16059G>T , LRG_141:g.16059G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*224G>T ENSP00000512122.1:n.*224G>T
ENST00000695725.1:c.*161G>T ENSP00000512123.1:n.*161G>T
ENST00000695726.1:n.2574G>T
ENST00000695729.1:n.3409G>T
ENST00000370629.7:c.606G>T MANE Select ENSP00000359663.2:p.Glu202Asp
ENST00000370628.2:c.543G>T ENSP00000359662.2:p.Glu181Asp
ENST00000370629.6:c.606G>T ENSP00000359663.2:p.Glu202Asp
NM_000074.2:c.606G>T , LRG_141t1:c.606G>T NP_000065.1:p.Glu202Asp
NM_000074.3:c.606G>T MANE Select NP_000065.1:p.Glu202Asp