Canonical Allele Identifier: CA1788120274
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60860847C= , CM000670.2:g.60860847C= GRCh38
NC_000008.10:g.61773406C= , CM000670.1:g.61773406C= GRCh37
NC_000008.9:g.61935960C= NCBI36
NG_007009.1:g.187068C= , LRG_176:g.187068C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695850.1:n.785-57C=
ENST00000695853.1:c.*668-57C= ENSP00000512218.1:n.*668-57C=
ENST00000423902.7:c.7609-57C= MANE Select ENSP00000392028.1:n.7609-57C=
ENST00000423902.6:c.7609-57C= ENSP00000392028.1:n.7609-57C=
ENST00000524602.5:c.1717-1382C= ENSP00000437061.1:n.1717-1382C=
ENST00000531695.1:n.33-57C=
NM_001316690.1:c.1717-1382C= NP_001303619.1:n.1717-1382C=
NM_017780.3:c.7609-57C= NP_060250.2:n.7609-57C=
XM_011517553.1:c.7699-57C= XP_011515855.1:n.7699-57C=
XM_011517554.1:c.7699-57C= XP_011515856.1:n.7699-57C=
XM_011517555.1:c.7696-57C= XP_011515857.1:n.7696-57C=
XM_011517556.1:c.7699-1349C= XP_011515858.1:n.7699-1349C=
XM_011517557.1:c.5686-57C= XP_011515859.1:n.5686-57C=
XM_011517558.1:c.5236-57C= XP_011515860.1:n.5236-57C=
XM_011517559.1:c.4444-57C= XP_011515861.1:n.4444-57C=
XM_011517553.2:c.7699-57C= XP_011515855.1:n.7699-57C=
XM_011517554.3:c.7699-57C= XP_011515856.1:n.7699-57C=
XM_011517555.2:c.7696-57C= XP_011515857.1:n.7696-57C=
XM_017013612.1:c.7699-57C= XP_016869101.1:n.7699-57C=
XM_017013613.1:c.7606-57C= XP_016869102.1:n.7606-57C=
NM_017780.4:c.7609-57C= MANE Select NP_060250.2:n.7609-57C=