Canonical Allele Identifier: CA409212237

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757642G>C (hg19) ; chr20:g.46129003G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129003G>C , CM000682.2:g.46129003G>C	GRCh38
NC_000020.10:g.44757642G>C , CM000682.1:g.44757642G>C	GRCh37
NC_000020.9:g.44191049G>C	NCBI36
NG_007279.1:g.15737G>C , LRG_40:g.15737G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.799G>C	ENSP00000512095.1:n.799G>C
ENST00000489304.6:c.880G>C	ENSP00000512096.1:n.880G>C
ENST00000695675.1:n.2673G>C
ENST00000372285.8:c.797G>C MANE Select	ENSP00000361359.3:p.Gly266Ala
ENST00000372276.7:c.*123G>C	ENSP00000361350.3:n.*123G>C
ENST00000372285.7:c.797G>C	ENSP00000361359.3:p.Gly266Ala
ENST00000466205.5:c.699G>C
ENST00000477696.5:n.770G>C
ENST00000489304.5:n.873G>C
ENST00000620709.4:c.*344G>C	ENSP00000484074.1:n.*344G>C
NM_001250.5:c.797G>C	NP_001241.1:p.Gly266Ala
NM_001302753.1:c.*123G>C	NP_001289682.1:n.*123G>C
NM_152854.3:c.*123G>C	NP_690593.1:n.*123G>C
NR_126502.1:n.890G>C
XM_005260617.2:c.809G>C	XP_005260674.1:p.Gly270Ala
XM_005260619.2:c.653G>C	XP_005260676.1:p.Gly218Ala
XR_936660.1:n.797G>C
NM_001322421.1:c.809G>C	NP_001309350.1:p.Gly270Ala
NM_001322422.1:c.641G>C	NP_001309351.1:p.Gly214Ala
NM_001362758.1:c.*123G>C	NP_001349687.1:n.*123G>C
NR_136327.1:n.793G>C
XM_005260619.3:c.653G>C	XP_005260676.1:p.Gly218Ala
XM_017028135.1:c.832G>C	XP_016883624.1:p.Ala278Pro
XM_017028136.1:c.730G>C	XP_016883625.1:p.Ala244Pro
NM_001250.6:c.797G>C MANE Select	NP_001241.1:p.Gly266Ala
NM_001302753.2:c.*123G>C	NP_001289682.1:n.*123G>C
NM_001322421.2:c.809G>C	NP_001309350.1:p.Gly270Ala
NM_001322422.2:c.641G>C	NP_001309351.1:p.Gly214Ala
NM_001362758.2:c.*123G>C	NP_001349687.1:n.*123G>C
NM_152854.4:c.*123G>C	NP_690593.1:n.*123G>C
NR_126502.2:n.830G>C
NR_136327.2:n.733G>C