Canonical Allele Identifier: CA271296
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 158287
dbSNP Id: rs587783436

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60822093_60822094del , CM000670.2:g.60822093_60822094del GRCh38
NC_000008.10:g.61734652_61734653del , CM000670.1:g.61734652_61734653del GRCh37
NC_000008.9:g.61897206_61897207del NCBI36
NG_007009.1:g.148314_148315del , LRG_176:g.148314_148315del

Transcript Alleles

HGVS Amino-acid change
ENST00000695853.1:c.2905_2906del ENSP00000512218.1:p.Arg969GlyfsTer25
ENST00000423902.7:c.2905_2906del MANE Select ENSP00000392028.1:p.Arg969GlyfsTer25
ENST00000423902.6:c.2905_2906del ENSP00000392028.1:p.Arg969GlyfsTer25
ENST00000524602.5:c.1717-40136_1717-40135del ENSP00000437061.1:n.1717-40136_1717-40135...
ENST00000525508.1:c.2905_2906del ENSP00000436027.1:p.Arg969GlyfsTer25
NM_001316690.1:c.1717-40136_1717-40135del NP_001303619.1:n.1717-40136_1717-40135del...
NM_017780.3:c.2905_2906del NP_060250.2:p.Arg969GlyfsTer25
XM_011517553.1:c.2905_2906del XP_011515855.1:p.Arg969GlyfsTer25
XM_011517554.1:c.2905_2906del XP_011515856.1:p.Arg969GlyfsTer25
XM_011517555.1:c.2905_2906del XP_011515857.1:p.Arg969GlyfsTer25
XM_011517556.1:c.2905_2906del XP_011515858.1:p.Arg969GlyfsTer25
XM_011517557.1:c.892_893del XP_011515859.1:p.Arg298GlyfsTer25
XM_011517558.1:c.442_443del XP_011515860.1:p.Arg148GlyfsTer25
XM_011517560.1:c.2905_2906del XP_011515862.1:p.Arg969GlyfsTer25
XM_011517553.2:c.2905_2906del XP_011515855.1:p.Arg969GlyfsTer25
XM_011517554.3:c.2905_2906del XP_011515856.1:p.Arg969GlyfsTer25
XM_011517555.2:c.2905_2906del XP_011515857.1:p.Arg969GlyfsTer25
XM_011517560.2:c.2905_2906del XP_011515862.1:p.Arg969GlyfsTer25
XM_017013612.1:c.2905_2906del XP_016869101.1:p.Arg969GlyfsTer25
XM_017013613.1:c.2905_2906del XP_016869102.1:p.Arg969GlyfsTer25
NM_017780.4:c.2905_2906del MANE Select NP_060250.2:p.Arg969GlyfsTer25