Canonical Allele Identifier: CA1788122822

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60841863_60841864delinsAT , CM000670.2:g.60841863_60841864delinsAT	GRCh38
NC_000008.10:g.61754422_61754423delinsAT , CM000670.1:g.61754422_61754423delinsAT	GRCh37
NC_000008.9:g.61916976_61916977delinsAT	NCBI36
NG_007009.1:g.168084_168085delinsAT , LRG_176:g.168084_168085delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.4661_4662delinsAT	ENSP00000512218.1:p.Asp1554=
ENST00000423902.7:c.4661_4662delinsAT MANE Select	ENSP00000392028.1:p.Asp1554=
ENST00000423902.6:c.4661_4662delinsAT	ENSP00000392028.1:p.Asp1554=
ENST00000524602.5:c.1717-20366_1717-20365delinsAT	ENSP00000437061.1:n.1717-20366_1717-20365delinsAT
NM_001316690.1:c.1717-20366_1717-20365delinsAT	NP_001303619.1:n.1717-20366_1717-20365delinsAT
NM_017780.3:c.4661_4662delinsAT	NP_060250.2:p.Asp1554=
XM_011517553.1:c.4661_4662delinsAT	XP_011515855.1:p.Asp1554=
XM_011517554.1:c.4661_4662delinsAT	XP_011515856.1:p.Asp1554=
XM_011517555.1:c.4661_4662delinsAT	XP_011515857.1:p.Asp1554=
XM_011517556.1:c.4661_4662delinsAT	XP_011515858.1:p.Asp1554=
XM_011517557.1:c.2648_2649delinsAT	XP_011515859.1:p.Asp883=
XM_011517558.1:c.2198_2199delinsAT	XP_011515860.1:p.Asp733=
XM_011517559.1:c.1406_1407delinsAT	XP_011515861.1:p.Asp469=
XM_011517560.1:c.4661_4662delinsAT	XP_011515862.1:p.Asp1554=
XM_011517553.2:c.4661_4662delinsAT	XP_011515855.1:p.Asp1554=
XM_011517554.3:c.4661_4662delinsAT	XP_011515856.1:p.Asp1554=
XM_011517555.2:c.4661_4662delinsAT	XP_011515857.1:p.Asp1554=
XM_011517560.2:c.4661_4662delinsAT	XP_011515862.1:p.Asp1554=
XM_017013612.1:c.4661_4662delinsAT	XP_016869101.1:p.Asp1554=
XM_017013613.1:c.4661_4662delinsAT	XP_016869102.1:p.Asp1554=
NM_017780.4:c.4661_4662delinsAT MANE Select	NP_060250.2:p.Asp1554=