Canonical Allele Identifier: CA1788120271
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60860846A= , CM000670.2:g.60860846A= GRCh38
NC_000008.10:g.61773405A= , CM000670.1:g.61773405A= GRCh37
NC_000008.9:g.61935959A= NCBI36
NG_007009.1:g.187067A= , LRG_176:g.187067A=

Transcript Alleles

HGVS Amino-acid change
ENST00000695850.1:n.785-58A=
ENST00000695853.1:c.*668-58A= ENSP00000512218.1:n.*668-58A=
ENST00000423902.7:c.7609-58A= MANE Select ENSP00000392028.1:n.7609-58A=
ENST00000423902.6:c.7609-58A= ENSP00000392028.1:n.7609-58A=
ENST00000524602.5:c.1717-1383A= ENSP00000437061.1:n.1717-1383A=
ENST00000531695.1:n.33-58A=
NM_001316690.1:c.1717-1383A= NP_001303619.1:n.1717-1383A=
NM_017780.3:c.7609-58A= NP_060250.2:n.7609-58A=
XM_011517553.1:c.7699-58A= XP_011515855.1:n.7699-58A=
XM_011517554.1:c.7699-58A= XP_011515856.1:n.7699-58A=
XM_011517555.1:c.7696-58A= XP_011515857.1:n.7696-58A=
XM_011517556.1:c.7699-1350A= XP_011515858.1:n.7699-1350A=
XM_011517557.1:c.5686-58A= XP_011515859.1:n.5686-58A=
XM_011517558.1:c.5236-58A= XP_011515860.1:n.5236-58A=
XM_011517559.1:c.4444-58A= XP_011515861.1:n.4444-58A=
XM_011517553.2:c.7699-58A= XP_011515855.1:n.7699-58A=
XM_011517554.3:c.7699-58A= XP_011515856.1:n.7699-58A=
XM_011517555.2:c.7696-58A= XP_011515857.1:n.7696-58A=
XM_017013612.1:c.7699-58A= XP_016869101.1:n.7699-58A=
XM_017013613.1:c.7606-58A= XP_016869102.1:n.7606-58A=
NM_017780.4:c.7609-58A= MANE Select NP_060250.2:n.7609-58A=