Canonical Allele Identifier: CA2695209397
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60852594del , CM000670.2:g.60852594del GRCh38
NC_000008.10:g.61765153del , CM000670.1:g.61765153del GRCh37
NC_000008.9:g.61927707del NCBI36
NG_007009.1:g.178815del , LRG_176:g.178815del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695853.1:c.5991del ENSP00000512218.1:p.Phe1997LeufsTer?
ENST00000423902.7:c.5991del MANE Select ENSP00000392028.1:p.Phe1997LeufsTer?
ENST00000423902.6:c.5991del ENSP00000392028.1:p.Phe1997LeufsTer?
ENST00000524602.5:c.1717-9635del ENSP00000437061.1:n.1717-9635del
ENST00000527921.1:n.482del
NM_001316690.1:c.1717-9635del NP_001303619.1:n.1717-9635del
NM_017780.3:c.5991del NP_060250.2:p.Phe1997LeufsTer?
XM_011517553.1:c.6081del XP_011515855.1:p.Phe2027LeufsTer?
XM_011517554.1:c.6081del XP_011515856.1:p.Phe2027LeufsTer?
XM_011517555.1:c.6081del XP_011515857.1:p.Phe2027LeufsTer?
XM_011517556.1:c.6081del XP_011515858.1:p.Phe2027LeufsTer?
XM_011517557.1:c.4068del XP_011515859.1:p.Phe1356LeufsTer?
XM_011517558.1:c.3618del XP_011515860.1:p.Phe1206LeufsTer?
XM_011517559.1:c.2826del XP_011515861.1:p.Phe942LeufsTer?
XM_011517553.2:c.6081del XP_011515855.1:p.Phe2027LeufsTer?
XM_011517554.3:c.6081del XP_011515856.1:p.Phe2027LeufsTer?
XM_011517555.2:c.6081del XP_011515857.1:p.Phe2027LeufsTer?
XM_017013612.1:c.6081del XP_016869101.1:p.Phe2027LeufsTer?
XM_017013613.1:c.5991del XP_016869102.1:p.Phe1997LeufsTer?
NM_017780.4:c.5991del MANE Select NP_060250.2:p.Phe1997LeufsTer?