Canonical Allele Identifier: CA518855938
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076127167
MyVariant Identifiers: chrX:g.135741325C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659166C>T , CM000685.2:g.136659166C>T GRCh38
NC_000023.10:g.135741325C>T , CM000685.1:g.135741325C>T GRCh37
NC_000023.9:g.135568991C>T NCBI36
NG_007280.1:g.15990C>T , LRG_141:g.15990C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*155C>T ENSP00000512122.1:n.*155C>T
ENST00000695725.1:c.*92C>T ENSP00000512123.1:n.*92C>T
ENST00000695726.1:n.2505C>T
ENST00000695729.1:n.3340C>T
ENST00000370629.7:c.537C>T MANE Select ENSP00000359663.2:p.Ser179=
ENST00000370628.2:c.474C>T ENSP00000359662.2:p.Ser158=
ENST00000370629.6:c.537C>T ENSP00000359663.2:p.Ser179=
NM_000074.2:c.537C>T , LRG_141t1:c.537C>T NP_000065.1:p.Ser179=
NM_000074.3:c.537C>T MANE Select NP_000065.1:p.Ser179=