Canonical Allele Identifier: CA414756319
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659278C>T , CM000685.2:g.136659278C>T GRCh38
NC_000023.10:g.135741437C>T , CM000685.1:g.135741437C>T GRCh37
NC_000023.9:g.135569103C>T NCBI36
NG_007280.1:g.16102C>T , LRG_141:g.16102C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*267C>T ENSP00000512122.1:n.*267C>T
ENST00000695725.1:c.*204C>T ENSP00000512123.1:n.*204C>T
ENST00000695726.1:n.2617C>T
ENST00000695729.1:n.3452C>T
ENST00000370629.7:c.649C>T MANE Select ENSP00000359663.2:p.Pro217Ser
ENST00000370628.2:c.586C>T ENSP00000359662.2:p.Pro196Ser
ENST00000370629.6:c.649C>T ENSP00000359663.2:p.Pro217Ser
NM_000074.2:c.649C>T , LRG_141t1:c.649C>T NP_000065.1:p.Pro217Ser
NM_000074.3:c.649C>T MANE Select NP_000065.1:p.Pro217Ser