Canonical Allele Identifier: CA2694818732

Gene: CD40LG

Linked Data

• gnomAD v4: X-136658921-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136658921G>T , CM000685.2:g.136658921G>T	GRCh38
NC_000023.10:g.135741080G>T , CM000685.1:g.135741080G>T	GRCh37
NC_000023.9:g.135568746G>T	NCBI36
NG_007280.1:g.15745G>T , LRG_141:g.15745G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*28-118G>T	ENSP00000512122.1:n.*28-118G>T
ENST00000695725.1:c.157-118G>T	ENSP00000512123.1:n.157-118G>T
ENST00000695726.1:n.2378-118G>T
ENST00000695729.1:n.3213-118G>T
ENST00000370629.7:c.410-118G>T MANE Select	ENSP00000359663.2:n.410-118G>T
ENST00000370628.2:c.347-118G>T	ENSP00000359662.2:n.347-118G>T
ENST00000370629.6:c.410-118G>T	ENSP00000359663.2:n.410-118G>T
NM_000074.2:c.410-118G>T , LRG_141t1:c.410-118G>T	NP_000065.1:n.410-118G>T
NM_000074.3:c.410-118G>T MANE Select	NP_000065.1:n.410-118G>T