Canonical Allele Identifier: CA518856083
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741547C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659388C>T , CM000685.2:g.136659388C>T GRCh38
NC_000023.10:g.135741547C>T , CM000685.1:g.135741547C>T GRCh37
NC_000023.9:g.135569213C>T NCBI36
NG_007280.1:g.16212C>T , LRG_141:g.16212C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*377C>T ENSP00000512122.1:n.*377C>T
ENST00000695725.1:c.*314C>T ENSP00000512123.1:n.*314C>T
ENST00000695726.1:n.2727C>T
ENST00000695729.1:n.3562C>T
ENST00000370629.7:c.759C>T MANE Select ENSP00000359663.2:p.Phe253=
ENST00000370628.2:c.696C>T ENSP00000359662.2:p.Phe232=
ENST00000370629.6:c.759C>T ENSP00000359663.2:p.Phe253=
NM_000074.2:c.759C>T , LRG_141t1:c.759C>T NP_000065.1:p.Phe253=
NM_000074.3:c.759C>T MANE Select NP_000065.1:p.Phe253=