Canonical Allele Identifier: CA4760773
Gene: CHD7 HGNC NCBI

Linked Data

dbSNP Id: rs374380640

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60856492_60856494dup , CM000670.2:g.60856492_60856494dup GRCh38
NC_000008.10:g.61769051_61769053dup , CM000670.1:g.61769051_61769053dup GRCh37
NC_000008.9:g.61931605_61931607dup NCBI36
NG_007009.1:g.182713_182715dup , LRG_176:g.182713_182715dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695850.1:n.388_390dup
ENST00000695853.1:c.*271_*273dup ENSP00000512218.1:n.*271_*273dup
ENST00000423902.7:c.7212_7214dup MANE Select ENSP00000392028.1:p.Arg2405_Lys2406insArg
ENST00000423902.6:c.7212_7214dup ENSP00000392028.1:p.Arg2405_Lys2406insArg
ENST00000524602.5:c.1717-5737_1717-5735dup ENSP00000437061.1:n.1717-5737_1717-5735dup
ENST00000529472.1:n.393_395dup
NM_001316690.1:c.1717-5737_1717-5735dup NP_001303619.1:n.1717-5737_1717-5735dup
NM_017780.3:c.7212_7214dup NP_060250.2:p.Arg2405_Lys2406insArg
XM_011517553.1:c.7302_7304dup XP_011515855.1:p.Arg2435_Lys2436insArg
XM_011517554.1:c.7302_7304dup XP_011515856.1:p.Arg2435_Lys2436insArg
XM_011517555.1:c.7299_7301dup XP_011515857.1:p.Arg2434_Lys2435insArg
XM_011517556.1:c.7302_7304dup XP_011515858.1:p.Arg2435_Lys2436insArg
XM_011517557.1:c.5289_5291dup XP_011515859.1:p.Arg1764_Lys1765insArg
XM_011517558.1:c.4839_4841dup XP_011515860.1:p.Arg1614_Lys1615insArg
XM_011517559.1:c.4047_4049dup XP_011515861.1:p.Arg1350_Lys1351insArg
XM_011517553.2:c.7302_7304dup XP_011515855.1:p.Arg2435_Lys2436insArg
XM_011517554.3:c.7302_7304dup XP_011515856.1:p.Arg2435_Lys2436insArg
XM_011517555.2:c.7299_7301dup XP_011515857.1:p.Arg2434_Lys2435insArg
XM_017013612.1:c.7302_7304dup XP_016869101.1:p.Arg2435_Lys2436insArg
XM_017013613.1:c.7209_7211dup XP_016869102.1:p.Arg2404_Lys2405insArg
NM_017780.4:c.7212_7214dup MANE Select NP_060250.2:p.Arg2405_Lys2406insArg