Canonical Allele Identifier: CA518856061
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741511G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659352G>T , CM000685.2:g.136659352G>T GRCh38
NC_000023.10:g.135741511G>T , CM000685.1:g.135741511G>T GRCh37
NC_000023.9:g.135569177G>T NCBI36
NG_007280.1:g.16176G>T , LRG_141:g.16176G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*341G>T ENSP00000512122.1:n.*341G>T
ENST00000695725.1:c.*278G>T ENSP00000512123.1:n.*278G>T
ENST00000695726.1:n.2691G>T
ENST00000695729.1:n.3526G>T
ENST00000370629.7:c.723G>T MANE Select ENSP00000359663.2:p.Val241=
ENST00000370628.2:c.660G>T ENSP00000359662.2:p.Val220=
ENST00000370629.6:c.723G>T ENSP00000359663.2:p.Val241=
NM_000074.2:c.723G>T , LRG_141t1:c.723G>T NP_000065.1:p.Val241=
NM_000074.3:c.723G>T MANE Select NP_000065.1:p.Val241=