Canonical Allele Identifier: CA1788120761

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860990A= , CM000670.2:g.60860990A=	GRCh38
NC_000008.10:g.61773549A= , CM000670.1:g.61773549A=	GRCh37
NC_000008.9:g.61936103A=	NCBI36
NG_007009.1:g.187211A= , LRG_176:g.187211A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.871A=
ENST00000695851.1:n.75A=
ENST00000695853.1:c.*754A=	ENSP00000512218.1:n.*754A=
ENST00000423902.7:c.7695A= MANE Select	ENSP00000392028.1:p.Pro2565=
ENST00000423902.6:c.7695A=	ENSP00000392028.1:p.Pro2565=
ENST00000524602.5:c.1717-1239A=	ENSP00000437061.1:n.1717-1239A=
ENST00000531695.1:n.119A=
ENST00000618450.1:n.87A=
NM_001316690.1:c.1717-1239A=	NP_001303619.1:n.1717-1239A=
NM_017780.3:c.7695A=	NP_060250.2:p.Pro2565=
XM_011517553.1:c.7785A=	XP_011515855.1:p.Pro2595=
XM_011517554.1:c.7785A=	XP_011515856.1:p.Pro2595=
XM_011517555.1:c.7782A=	XP_011515857.1:p.Pro2594=
XM_011517556.1:c.7699-1206A=	XP_011515858.1:n.7699-1206A=
XM_011517557.1:c.5772A=	XP_011515859.1:p.Pro1924=
XM_011517558.1:c.5322A=	XP_011515860.1:p.Pro1774=
XM_011517559.1:c.4530A=	XP_011515861.1:p.Pro1510=
XM_011517553.2:c.7785A=	XP_011515855.1:p.Pro2595=
XM_011517554.3:c.7785A=	XP_011515856.1:p.Pro2595=
XM_011517555.2:c.7782A=	XP_011515857.1:p.Pro2594=
XM_017013612.1:c.7785A=	XP_016869101.1:p.Pro2595=
XM_017013613.1:c.7692A=	XP_016869102.1:p.Pro2564=
NM_017780.4:c.7695A= MANE Select	NP_060250.2:p.Pro2565=