Canonical Allele Identifier: CA518856057

Gene: CD40LG

Linked Data

• COSMIC: COSM5024449
• MyVariant Identifiers: chrX:g.135741505C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659346C>T , CM000685.2:g.136659346C>T	GRCh38
NC_000023.10:g.135741505C>T , CM000685.1:g.135741505C>T	GRCh37
NC_000023.9:g.135569171C>T	NCBI36
NG_007280.1:g.16170C>T , LRG_141:g.16170C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*335C>T	ENSP00000512122.1:n.*335C>T
ENST00000695725.1:c.*272C>T	ENSP00000512123.1:n.*272C>T
ENST00000695726.1:n.2685C>T
ENST00000695729.1:n.3520C>T
ENST00000370629.7:c.717C>T MANE Select	ENSP00000359663.2:p.Val239=
ENST00000370628.2:c.654C>T	ENSP00000359662.2:p.Val218=
ENST00000370629.6:c.717C>T	ENSP00000359663.2:p.Val239=
NM_000074.2:c.717C>T , LRG_141t1:c.717C>T	NP_000065.1:p.Val239=
NM_000074.3:c.717C>T MANE Select	NP_000065.1:p.Val239=