Canonical Allele Identifier: CA510657869

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757643C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129004C>G , CM000682.2:g.46129004C>G	GRCh38
NC_000020.10:g.44757643C>G , CM000682.1:g.44757643C>G	GRCh37
NC_000020.9:g.44191050C>G	NCBI36
NG_007279.1:g.15738C>G , LRG_40:g.15738C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.800C>G	ENSP00000512095.1:n.800C>G
ENST00000489304.6:c.881C>G	ENSP00000512096.1:n.881C>G
ENST00000695675.1:n.2674C>G
ENST00000372285.8:c.798C>G MANE Select	ENSP00000361359.3:p.Gly266=
ENST00000372276.7:c.*124C>G	ENSP00000361350.3:n.*124C>G
ENST00000372285.7:c.798C>G	ENSP00000361359.3:p.Gly266=
ENST00000466205.5:c.700C>G
ENST00000477696.5:n.771C>G
ENST00000489304.5:n.874C>G
ENST00000620709.4:c.*345C>G	ENSP00000484074.1:n.*345C>G
NM_001250.5:c.798C>G	NP_001241.1:p.Gly266=
NM_001302753.1:c.*124C>G	NP_001289682.1:n.*124C>G
NM_152854.3:c.*124C>G	NP_690593.1:n.*124C>G
NR_126502.1:n.891C>G
XM_005260617.2:c.810C>G	XP_005260674.1:p.Gly270=
XM_005260619.2:c.654C>G	XP_005260676.1:p.Gly218=
XR_936660.1:n.798C>G
NM_001322421.1:c.810C>G	NP_001309350.1:p.Gly270=
NM_001322422.1:c.642C>G	NP_001309351.1:p.Gly214=
NM_001362758.1:c.*124C>G	NP_001349687.1:n.*124C>G
NR_136327.1:n.794C>G
XM_005260619.3:c.654C>G	XP_005260676.1:p.Gly218=
XM_017028135.1:c.833C>G	XP_016883624.1:p.Ala278Gly
XM_017028136.1:c.731C>G	XP_016883625.1:p.Ala244Gly
NM_001250.6:c.798C>G MANE Select	NP_001241.1:p.Gly266=
NM_001302753.2:c.*124C>G	NP_001289682.1:n.*124C>G
NM_001322421.2:c.810C>G	NP_001309350.1:p.Gly270=
NM_001322422.2:c.642C>G	NP_001309351.1:p.Gly214=
NM_001362758.2:c.*124C>G	NP_001349687.1:n.*124C>G
NM_152854.4:c.*124C>G	NP_690593.1:n.*124C>G
NR_126502.2:n.831C>G
NR_136327.2:n.734C>G