Canonical Allele Identifier: CA414756057
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076127566

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659233G>C , CM000685.2:g.136659233G>C GRCh38
NC_000023.10:g.135741392G>C , CM000685.1:g.135741392G>C GRCh37
NC_000023.9:g.135569058G>C NCBI36
NG_007280.1:g.16057G>C , LRG_141:g.16057G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*222G>C ENSP00000512122.1:n.*222G>C
ENST00000695725.1:c.*159G>C ENSP00000512123.1:n.*159G>C
ENST00000695726.1:n.2572G>C
ENST00000695729.1:n.3407G>C
ENST00000370629.7:c.604G>C MANE Select ENSP00000359663.2:p.Glu202Gln
ENST00000370628.2:c.541G>C ENSP00000359662.2:p.Glu181Gln
ENST00000370629.6:c.604G>C ENSP00000359663.2:p.Glu202Gln
NM_000074.2:c.604G>C , LRG_141t1:c.604G>C NP_000065.1:p.Glu202Gln
NM_000074.3:c.604G>C MANE Select NP_000065.1:p.Glu202Gln