Canonical Allele Identifier: CA518856013
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741439T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659280T>A , CM000685.2:g.136659280T>A GRCh38
NC_000023.10:g.135741439T>A , CM000685.1:g.135741439T>A GRCh37
NC_000023.9:g.135569105T>A NCBI36
NG_007280.1:g.16104T>A , LRG_141:g.16104T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*269T>A ENSP00000512122.1:n.*269T>A
ENST00000695725.1:c.*206T>A ENSP00000512123.1:n.*206T>A
ENST00000695726.1:n.2619T>A
ENST00000695729.1:n.3454T>A
ENST00000370629.7:c.651T>A MANE Select ENSP00000359663.2:p.Pro217=
ENST00000370628.2:c.588T>A ENSP00000359662.2:p.Pro196=
ENST00000370629.6:c.651T>A ENSP00000359663.2:p.Pro217=
NM_000074.2:c.651T>A , LRG_141t1:c.651T>A NP_000065.1:p.Pro217=
NM_000074.3:c.651T>A MANE Select NP_000065.1:p.Pro217=
Search 100 bp 5'
Search 100 bp 3'