Canonical Allele Identifier: CA1788120869

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861037T= , CM000670.2:g.60861037T=	GRCh38
NC_000008.10:g.61773596T= , CM000670.1:g.61773596T=	GRCh37
NC_000008.9:g.61936150T=	NCBI36
NG_007009.1:g.187258T= , LRG_176:g.187258T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.918T=
ENST00000695851.1:n.122T=
ENST00000695853.1:c.*801T=	ENSP00000512218.1:n.*801T=
ENST00000423902.7:c.7742T= MANE Select	ENSP00000392028.1:p.Val2581=
ENST00000423902.6:c.7742T=	ENSP00000392028.1:p.Val2581=
ENST00000524602.5:c.1717-1192T=	ENSP00000437061.1:n.1717-1192T=
ENST00000531695.1:n.166T=
ENST00000618450.1:n.134T=
NM_001316690.1:c.1717-1192T=	NP_001303619.1:n.1717-1192T=
NM_017780.3:c.7742T=	NP_060250.2:p.Val2581=
XM_011517553.1:c.7832T=	XP_011515855.1:p.Val2611=
XM_011517554.1:c.7832T=	XP_011515856.1:p.Val2611=
XM_011517555.1:c.7829T=	XP_011515857.1:p.Val2610=
XM_011517556.1:c.7699-1159T=	XP_011515858.1:n.7699-1159T=
XM_011517557.1:c.5819T=	XP_011515859.1:p.Val1940=
XM_011517558.1:c.5369T=	XP_011515860.1:p.Val1790=
XM_011517559.1:c.4577T=	XP_011515861.1:p.Val1526=
XM_011517553.2:c.7832T=	XP_011515855.1:p.Val2611=
XM_011517554.3:c.7832T=	XP_011515856.1:p.Val2611=
XM_011517555.2:c.7829T=	XP_011515857.1:p.Val2610=
XM_017013612.1:c.7832T=	XP_016869101.1:p.Val2611=
XM_017013613.1:c.7739T=	XP_016869102.1:p.Val2580=
NM_017780.4:c.7742T= MANE Select	NP_060250.2:p.Val2581=