Canonical Allele Identifier: CA414756710
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659341T>C , CM000685.2:g.136659341T>C GRCh38
NC_000023.10:g.135741500T>C , CM000685.1:g.135741500T>C GRCh37
NC_000023.9:g.135569166T>C NCBI36
NG_007280.1:g.16165T>C , LRG_141:g.16165T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*330T>C ENSP00000512122.1:n.*330T>C
ENST00000695725.1:c.*267T>C ENSP00000512123.1:n.*267T>C
ENST00000695726.1:n.2680T>C
ENST00000695729.1:n.3515T>C
ENST00000370629.7:c.712T>C MANE Select ENSP00000359663.2:p.Phe238Leu
ENST00000370628.2:c.649T>C ENSP00000359662.2:p.Phe217Leu
ENST00000370629.6:c.712T>C ENSP00000359663.2:p.Phe238Leu
NM_000074.2:c.712T>C , LRG_141t1:c.712T>C NP_000065.1:p.Phe238Leu
NM_000074.3:c.712T>C MANE Select NP_000065.1:p.Phe238Leu