Canonical Allele Identifier: CA353723

Gene: CD40LG

Linked Data

• PubMed: PMID:7678782

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.[136656393T>A;136656395A>G] , CM000685.2:g.[136656393T>A;136656395A>G]	GRCh38
NC_000023.10:g.[135738552T>A;135738554A>G] , CM000685.1:g.[135738552T>A;135738554A>G]	GRCh37
NC_000023.9:g.[135566218T>A;135566220A>G]	NCBI36
NG_007280.1:g.[13217T>A;13219A>G] , LRG_141:g.[13217T>A;13219A>G]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.[*2T>A;*4A>G]	ENSP00000512122.1:n.[*2T>A;*4A>G]
ENST00000695725.1:c.[157-2646T>A;157-2644A>G]	ENSP00000512123.1:n.[157-2646T>A;157-2644A>G]
ENST00000695726.1:n.[2352T>A;2354A>G]
ENST00000695729.1:n.[3187T>A;3189A>G]
ENST00000370629.7:c.[384T>A;386A>G] MANE Select	ENSP00000359663.2:p.[Ser128Arg;Glu129Gly]
ENST00000370628.2:c.[346+1963T>A;346+1965A>G]	ENSP00000359662.2:n.[346+1963T>A;346+1965A>G]
ENST00000370629.6:c.[384T>A;386A>G]	ENSP00000359663.2:p.Ser128_Glu129delinsArgTrp
NM_000074.2:c.[384T>A;386A>G] , LRG_141t1:c.[384T>A;386A>G]	NP_000065.1:p.[Ser128Arg;Glu129Gly]
NM_000074.3:c.[384T>A;386A>G] MANE Select	NP_000065.1:p.[Ser128Arg;Glu129Gly]