Canonical Allele Identifier: CA409205400
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122706G>T , CM000682.2:g.46122706G>T GRCh38
NC_000020.10:g.44751345G>T , CM000682.1:g.44751345G>T GRCh37
NC_000020.9:g.44184752G>T NCBI36
NG_007279.1:g.9440G>T , LRG_40:g.9440G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.449G>T ENSP00000512095.1:n.449G>T
ENST00000489304.6:c.353G>T ENSP00000512096.1:p.Ser118Ile
ENST00000695669.1:n.426G>T
ENST00000695670.1:n.333G>T
ENST00000695671.1:c.353G>T ENSP00000512093.1:p.Ser118Ile
ENST00000695672.1:n.278G>T
ENST00000695673.1:n.218G>T
ENST00000372285.8:c.353G>T MANE Select ENSP00000361359.3:p.Ser118Ile
ENST00000372276.7:c.353G>T ENSP00000361350.3:p.Ser118Ile
ENST00000372285.7:c.353G>T ENSP00000361359.3:p.Ser118Ile
ENST00000461171.1:n.138G>T
ENST00000466205.5:c.349G>T
ENST00000477696.5:n.420G>T
ENST00000489304.5:n.346G>T
ENST00000620709.4:c.353G>T ENSP00000484074.1:p.Ser118Ile
NM_001250.5:c.353G>T NP_001241.1:p.Ser118Ile
NM_001302753.1:c.353G>T NP_001289682.1:p.Ser118Ile
NM_152854.3:c.353G>T NP_690593.1:p.Ser118Ile
NR_126502.1:n.443G>T
XM_005260617.2:c.353G>T XP_005260674.1:p.Ser118Ile
XM_005260619.2:c.353G>T XP_005260676.1:p.Ser118Ile
XM_011529109.1:c.353G>T XP_011527411.1:p.Ser118Ile
XR_936660.1:n.447G>T
NM_001322421.1:c.353G>T NP_001309350.1:p.Ser118Ile
NM_001322422.1:c.353G>T NP_001309351.1:p.Ser118Ile
NM_001362758.1:c.353G>T NP_001349687.1:p.Ser118Ile
NR_136327.1:n.443G>T
XM_005260619.3:c.353G>T XP_005260676.1:p.Ser118Ile
XM_011529109.2:c.353G>T XP_011527411.1:p.Ser118Ile
XM_017028135.1:c.353G>T XP_016883624.1:p.Ser118Ile
XM_017028136.1:c.353G>T XP_016883625.1:p.Ser118Ile
NM_001250.6:c.353G>T MANE Select NP_001241.1:p.Ser118Ile
NM_001302753.2:c.353G>T NP_001289682.1:p.Ser118Ile
NM_001322421.2:c.353G>T NP_001309350.1:p.Ser118Ile
NM_001322422.2:c.353G>T NP_001309351.1:p.Ser118Ile
NM_001362758.2:c.353G>T NP_001349687.1:p.Ser118Ile
NM_152854.4:c.353G>T NP_690593.1:p.Ser118Ile
NR_126502.2:n.383G>T
NR_136327.2:n.383G>T