Canonical Allele Identifier: CA2846182873
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60841816_60841817del , CM000670.2:g.60841816_60841817del GRCh38
NC_000008.10:g.61754375_61754376del , CM000670.1:g.61754375_61754376del GRCh37
NC_000008.9:g.61916929_61916930del NCBI36
NG_007009.1:g.168037_168038del , LRG_176:g.168037_168038del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695853.1:c.4645-31_4645-30del ENSP00000512218.1:n.4645-31_4645-30del
ENST00000423902.7:c.4645-31_4645-30del MANE Select ENSP00000392028.1:n.4645-31_4645-30del
ENST00000423902.6:c.4645-31_4645-30del ENSP00000392028.1:n.4645-31_4645-30del
ENST00000524602.5:c.1717-20413_1717-20412del ENSP00000437061.1:n.1717-20413_1717-20412del
NM_001316690.1:c.1717-20413_1717-20412del NP_001303619.1:n.1717-20413_1717-20412del
NM_017780.3:c.4645-31_4645-30del NP_060250.2:n.4645-31_4645-30del
XM_011517553.1:c.4645-31_4645-30del XP_011515855.1:n.4645-31_4645-30del
XM_011517554.1:c.4645-31_4645-30del XP_011515856.1:n.4645-31_4645-30del
XM_011517555.1:c.4645-31_4645-30del XP_011515857.1:n.4645-31_4645-30del
XM_011517556.1:c.4645-31_4645-30del XP_011515858.1:n.4645-31_4645-30del
XM_011517557.1:c.2632-31_2632-30del XP_011515859.1:n.2632-31_2632-30del
XM_011517558.1:c.2182-31_2182-30del XP_011515860.1:n.2182-31_2182-30del
XM_011517559.1:c.1390-31_1390-30del XP_011515861.1:n.1390-31_1390-30del
XM_011517560.1:c.4645-31_4645-30del XP_011515862.1:n.4645-31_4645-30del
XM_011517553.2:c.4645-31_4645-30del XP_011515855.1:n.4645-31_4645-30del
XM_011517554.3:c.4645-31_4645-30del XP_011515856.1:n.4645-31_4645-30del
XM_011517555.2:c.4645-31_4645-30del XP_011515857.1:n.4645-31_4645-30del
XM_011517560.2:c.4645-31_4645-30del XP_011515862.1:n.4645-31_4645-30del
XM_017013612.1:c.4645-31_4645-30del XP_016869101.1:n.4645-31_4645-30del
XM_017013613.1:c.4645-31_4645-30del XP_016869102.1:n.4645-31_4645-30del
NM_017780.4:c.4645-31_4645-30del MANE Select NP_060250.2:n.4645-31_4645-30del