Canonical Allele Identifier: CA414756676
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659335T>G , CM000685.2:g.136659335T>G GRCh38
NC_000023.10:g.135741494T>G , CM000685.1:g.135741494T>G GRCh37
NC_000023.9:g.135569160T>G NCBI36
NG_007280.1:g.16159T>G , LRG_141:g.16159T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*324T>G ENSP00000512122.1:n.*324T>G
ENST00000695725.1:c.*261T>G ENSP00000512123.1:n.*261T>G
ENST00000695726.1:n.2674T>G
ENST00000695729.1:n.3509T>G
ENST00000370629.7:c.706T>G MANE Select ENSP00000359663.2:p.Ser236Ala
ENST00000370628.2:c.643T>G ENSP00000359662.2:p.Ser215Ala
ENST00000370629.6:c.706T>G ENSP00000359663.2:p.Ser236Ala
NM_000074.2:c.706T>G , LRG_141t1:c.706T>G NP_000065.1:p.Ser236Ala
NM_000074.3:c.706T>G MANE Select NP_000065.1:p.Ser236Ala