Canonical Allele Identifier: CA2739094609

Gene: CD40LG

Linked Data

• dbSNP Id: rs2148550638

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648559_136648565del , CM000685.2:g.136648559_136648565del	GRCh38
NC_000023.10:g.135730718_135730724del , CM000685.1:g.135730718_135730724del	GRCh37
NC_000023.9:g.135558384_135558390del	NCBI36
NG_007280.1:g.5383_5389del , LRG_141:g.5383_5389del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.156+155_156+161del	ENSP00000512122.1:n.156+155_156+161del
ENST00000695725.1:c.156+155_156+161del	ENSP00000512123.1:n.156+155_156+161del
ENST00000695726.1:n.199+155_199+161del
ENST00000695727.1:n.143+155_143+161del
ENST00000695728.1:n.143+155_143+161del
ENST00000370629.7:c.156+155_156+161del MANE Select	ENSP00000359663.2:n.156+155_156+161del
ENST00000370628.2:c.156+155_156+161del	ENSP00000359662.2:n.156+155_156+161del
ENST00000370629.6:c.156+155_156+161del	ENSP00000359663.2:n.156+155_156+161del
NM_000074.2:c.156+155_156+161del , LRG_141t1:c.156+155_156+161del	NP_000065.1:n.156+155_156+161del
NM_000074.3:c.156+155_156+161del MANE Select	NP_000065.1:n.156+155_156+161del