Canonical Allele Identifier: CA2695236773
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659140_136659142del , CM000685.2:g.136659140_136659142del GRCh38
NC_000023.10:g.135741299_135741301del , CM000685.1:g.135741299_135741301del GRCh37
NC_000023.9:g.135568965_135568967del NCBI36
NG_007280.1:g.15964_15966del , LRG_141:g.15964_15966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*129_*131del ENSP00000512122.1:n.*129_*131del
ENST00000695725.1:c.*66_*68del ENSP00000512123.1:n.*66_*68del
ENST00000695726.1:n.2479_2481del
ENST00000695729.1:n.3314_3316del
ENST00000370629.7:c.511_513del MANE Select ENSP00000359663.2:p.Ile171del
ENST00000370628.2:c.448_450del ENSP00000359662.2:p.Ile150del
ENST00000370629.6:c.511_513del ENSP00000359663.2:p.Ile171del
NM_000074.2:c.511_513del , LRG_141t1:c.511_513del NP_000065.1:p.Ile171del
NM_000074.3:c.511_513del MANE Select NP_000065.1:p.Ile171del