Canonical Allele Identifier: CA1788120574

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860946A= , CM000670.2:g.60860946A=	GRCh38
NC_000008.10:g.61773505A= , CM000670.1:g.61773505A=	GRCh37
NC_000008.9:g.61936059A=	NCBI36
NG_007009.1:g.187167A= , LRG_176:g.187167A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.827A=
ENST00000695851.1:n.31A=
ENST00000695853.1:c.*710A=	ENSP00000512218.1:n.*710A=
ENST00000423902.7:c.7651A= MANE Select	ENSP00000392028.1:p.Thr2551=
ENST00000423902.6:c.7651A=	ENSP00000392028.1:p.Thr2551=
ENST00000524602.5:c.1717-1283A=	ENSP00000437061.1:n.1717-1283A=
ENST00000531695.1:n.75A=
ENST00000618450.1:n.43A=
NM_001316690.1:c.1717-1283A=	NP_001303619.1:n.1717-1283A=
NM_017780.3:c.7651A=	NP_060250.2:p.Thr2551=
XM_011517553.1:c.7741A=	XP_011515855.1:p.Thr2581=
XM_011517554.1:c.7741A=	XP_011515856.1:p.Thr2581=
XM_011517555.1:c.7738A=	XP_011515857.1:p.Thr2580=
XM_011517556.1:c.7699-1250A=	XP_011515858.1:n.7699-1250A=
XM_011517557.1:c.5728A=	XP_011515859.1:p.Thr1910=
XM_011517558.1:c.5278A=	XP_011515860.1:p.Thr1760=
XM_011517559.1:c.4486A=	XP_011515861.1:p.Thr1496=
XM_011517553.2:c.7741A=	XP_011515855.1:p.Thr2581=
XM_011517554.3:c.7741A=	XP_011515856.1:p.Thr2581=
XM_011517555.2:c.7738A=	XP_011515857.1:p.Thr2580=
XM_017013612.1:c.7741A=	XP_016869101.1:p.Thr2581=
XM_017013613.1:c.7648A=	XP_016869102.1:p.Thr2550=
NM_017780.4:c.7651A= MANE Select	NP_060250.2:p.Thr2551=