Canonical Allele Identifier: CA518855972
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741373A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659214A>T , CM000685.2:g.136659214A>T GRCh38
NC_000023.10:g.135741373A>T , CM000685.1:g.135741373A>T GRCh37
NC_000023.9:g.135569039A>T NCBI36
NG_007280.1:g.16038A>T , LRG_141:g.16038A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*203A>T ENSP00000512122.1:n.*203A>T
ENST00000695725.1:c.*140A>T ENSP00000512123.1:n.*140A>T
ENST00000695726.1:n.2553A>T
ENST00000695729.1:n.3388A>T
ENST00000370629.7:c.585A>T MANE Select ENSP00000359663.2:p.Leu195=
ENST00000370628.2:c.522A>T ENSP00000359662.2:p.Leu174=
ENST00000370629.6:c.585A>T ENSP00000359663.2:p.Leu195=
NM_000074.2:c.585A>T , LRG_141t1:c.585A>T NP_000065.1:p.Leu195=
NM_000074.3:c.585A>T MANE Select NP_000065.1:p.Leu195=