Canonical Allele Identifier: CA414751518

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135730442C>T (hg19) ; chrX:g.136648283C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648283C>T , CM000685.2:g.136648283C>T	GRCh38
NC_000023.10:g.135730442C>T , CM000685.1:g.135730442C>T	GRCh37
NC_000023.9:g.135558108C>T	NCBI36
NG_007280.1:g.5107C>T , LRG_141:g.5107C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.35C>T	ENSP00000512122.1:p.Ser12Phe
ENST00000695725.1:c.35C>T	ENSP00000512123.1:p.Ser12Phe
ENST00000695726.1:n.78C>T
ENST00000695727.1:n.22C>T
ENST00000695728.1:n.22C>T
ENST00000370629.7:c.35C>T MANE Select	ENSP00000359663.2:p.Ser12Phe
ENST00000370628.2:c.35C>T	ENSP00000359662.2:p.Ser12Phe
ENST00000370629.6:c.35C>T	ENSP00000359663.2:p.Ser12Phe
NM_000074.2:c.35C>T , LRG_141t1:c.35C>T	NP_000065.1:p.Ser12Phe
NM_000074.3:c.35C>T MANE Select	NP_000065.1:p.Ser12Phe