Canonical Allele Identifier: CA2694818731
Gene: CD40LG HGNC NCBI

Linked Data

gnomAD v4: X-136658920-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136658920G>C , CM000685.2:g.136658920G>C GRCh38
NC_000023.10:g.135741079G>C , CM000685.1:g.135741079G>C GRCh37
NC_000023.9:g.135568745G>C NCBI36
NG_007280.1:g.15744G>C , LRG_141:g.15744G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*28-119G>C ENSP00000512122.1:n.*28-119G>C
ENST00000695725.1:c.157-119G>C ENSP00000512123.1:n.157-119G>C
ENST00000695726.1:n.2378-119G>C
ENST00000695729.1:n.3213-119G>C
ENST00000370629.7:c.410-119G>C MANE Select ENSP00000359663.2:n.410-119G>C
ENST00000370628.2:c.347-119G>C ENSP00000359662.2:n.347-119G>C
ENST00000370629.6:c.410-119G>C ENSP00000359663.2:n.410-119G>C
NM_000074.2:c.410-119G>C , LRG_141t1:c.410-119G>C NP_000065.1:n.410-119G>C
NM_000074.3:c.410-119G>C MANE Select NP_000065.1:n.410-119G>C
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