Canonical Allele Identifier: CA518782427
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741573G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659414G>A , CM000685.2:g.136659414G>A GRCh38
NC_000023.10:g.135741573G>A , CM000685.1:g.135741573G>A GRCh37
NC_000023.9:g.135569239G>A NCBI36
NG_007280.1:g.16238G>A , LRG_141:g.16238G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*403G>A ENSP00000512122.1:n.*403G>A
ENST00000695725.1:c.*340G>A ENSP00000512123.1:n.*340G>A
ENST00000695726.1:n.2753G>A
ENST00000695729.1:n.3588G>A
ENST00000370629.7:c.785G>A MANE Select ENSP00000359663.2:p.Ter262=
ENST00000370628.2:c.722G>A ENSP00000359662.2:p.Ter241=
ENST00000370629.6:c.785G>A ENSP00000359663.2:p.Ter262=
NM_000074.2:c.785G>A , LRG_141t1:c.785G>A NP_000065.1:p.Ter262=
NM_000074.3:c.785G>A MANE Select NP_000065.1:p.Ter262=
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