Canonical Allele Identifier: CA518856065
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741517T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659358T>C , CM000685.2:g.136659358T>C GRCh38
NC_000023.10:g.135741517T>C , CM000685.1:g.135741517T>C GRCh37
NC_000023.9:g.135569183T>C NCBI36
NG_007280.1:g.16182T>C , LRG_141:g.16182T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*347T>C ENSP00000512122.1:n.*347T>C
ENST00000695725.1:c.*284T>C ENSP00000512123.1:n.*284T>C
ENST00000695726.1:n.2697T>C
ENST00000695729.1:n.3532T>C
ENST00000370629.7:c.729T>C MANE Select ENSP00000359663.2:p.Asp243=
ENST00000370628.2:c.666T>C ENSP00000359662.2:p.Asp222=
ENST00000370629.6:c.729T>C ENSP00000359663.2:p.Asp243=
NM_000074.2:c.729T>C , LRG_141t1:c.729T>C NP_000065.1:p.Asp243=
NM_000074.3:c.729T>C MANE Select NP_000065.1:p.Asp243=
Search 100 bp 5'
Search 100 bp 3'