Canonical Allele Identifier: CA744874713

Gene: CD40

Linked Data

• dbSNP Id: rs1326310569
• gnomAD v3: 20-46122140-CCCCTA-C
• gnomAD v4: 20-46122140-CCCCTA-C
• MyVariant Identifiers: chr20:g.44750780_44750784del (hg19) ; chr20:g.46122141_46122145del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46122146_46122150del , CM000682.2:g.46122146_46122150del	GRCh38
NC_000020.10:g.44750785_44750789del , CM000682.1:g.44750785_44750789del	GRCh37
NC_000020.9:g.44184192_44184196del	NCBI36
NG_007279.1:g.8880_8884del , LRG_40:g.8880_8884del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.227-87_227-83del	ENSP00000512095.1:n.227-87_227-83del
ENST00000489304.6:c.131-87_131-83del	ENSP00000512096.1:n.131-87_131-83del
ENST00000695669.1:n.204-87_204-83del
ENST00000695670.1:n.111-87_111-83del
ENST00000695671.1:c.131-87_131-83del	ENSP00000512093.1:n.131-87_131-83del
ENST00000695672.1:n.56-87_56-83del
ENST00000372285.8:c.131-87_131-83del MANE Select	ENSP00000361359.3:n.131-87_131-83del
ENST00000372276.7:c.131-87_131-83del	ENSP00000361350.3:n.131-87_131-83del
ENST00000372285.7:c.131-87_131-83del	ENSP00000361359.3:n.131-87_131-83del
ENST00000466205.5:c.127-87_127-83del
ENST00000477696.5:n.198-87_198-83del
ENST00000489304.5:n.124-87_124-83del
ENST00000620709.4:c.131-87_131-83del	ENSP00000484074.1:n.131-87_131-83del
NM_001250.5:c.131-87_131-83del	NP_001241.1:n.131-87_131-83del
NM_001302753.1:c.131-87_131-83del	NP_001289682.1:n.131-87_131-83del
NM_152854.3:c.131-87_131-83del	NP_690593.1:n.131-87_131-83del
NR_126502.1:n.221-87_221-83del
XM_005260617.2:c.131-87_131-83del	XP_005260674.1:n.131-87_131-83del
XM_005260619.2:c.131-87_131-83del	XP_005260676.1:n.131-87_131-83del
XM_011529109.1:c.131-87_131-83del	XP_011527411.1:n.131-87_131-83del
XR_936660.1:n.225-87_225-83del
NM_001322421.1:c.131-87_131-83del	NP_001309350.1:n.131-87_131-83del
NM_001322422.1:c.131-87_131-83del	NP_001309351.1:n.131-87_131-83del
NM_001362758.1:c.131-87_131-83del	NP_001349687.1:n.131-87_131-83del
NR_136327.1:n.221-87_221-83del
XM_005260619.3:c.131-87_131-83del	XP_005260676.1:n.131-87_131-83del
XM_011529109.2:c.131-87_131-83del	XP_011527411.1:n.131-87_131-83del
XM_017028135.1:c.131-87_131-83del	XP_016883624.1:n.131-87_131-83del
XM_017028136.1:c.131-87_131-83del	XP_016883625.1:n.131-87_131-83del
NM_001250.6:c.131-87_131-83del MANE Select	NP_001241.1:n.131-87_131-83del
NM_001302753.2:c.131-87_131-83del	NP_001289682.1:n.131-87_131-83del
NM_001322421.2:c.131-87_131-83del	NP_001309350.1:n.131-87_131-83del
NM_001322422.2:c.131-87_131-83del	NP_001309351.1:n.131-87_131-83del
NM_001362758.2:c.131-87_131-83del	NP_001349687.1:n.131-87_131-83del
NM_152854.4:c.131-87_131-83del	NP_690593.1:n.131-87_131-83del
NR_126502.2:n.161-87_161-83del
NR_136327.2:n.161-87_161-83del