Canonical Allele Identifier: CA2739094187
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2148550505

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648202_136648207dup , CM000685.2:g.136648202_136648207dup GRCh38
NC_000023.10:g.135730361_135730366dup , CM000685.1:g.135730361_135730366dup GRCh37
NC_000023.9:g.135558027_135558032dup NCBI36
NG_007280.1:g.5026_5031dup , LRG_141:g.5026_5031dup

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-47_-42dup ENSP00000512122.1:n.-47_-42dup
ENST00000695725.1:c.-47_-42dup ENSP00000512123.1:n.-47_-42dup
ENST00000370629.7:c.-47_-42dup MANE Select ENSP00000359663.2:n.-47_-42dup
ENST00000370629.6:c.-47_-42dup ENSP00000359663.2:n.-47_-42dup
NM_000074.2:c.-47_-42dup , LRG_141t1:c.-47_-42dup NP_000065.1:n.-47_-42dup
NM_000074.3:c.-47_-42dup MANE Select NP_000065.1:n.-47_-42dup