Canonical Allele Identifier: CA1788112198

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60836023G= , CM000670.2:g.60836023G=	GRCh38
NC_000008.10:g.61748582G= , CM000670.1:g.61748582G=	GRCh37
NC_000008.9:g.61911136G=	NCBI36
NG_007009.1:g.162244G= , LRG_176:g.162244G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695853.1:c.3779-50G=	ENSP00000512218.1:n.3779-50G=
ENST00000423902.7:c.3779-50G= MANE Select	ENSP00000392028.1:n.3779-50G=
ENST00000423902.6:c.3779-50G=	ENSP00000392028.1:n.3779-50G=
ENST00000524602.5:c.1717-26206G=	ENSP00000437061.1:n.1717-26206G=
NM_001316690.1:c.1717-26206G=	NP_001303619.1:n.1717-26206G=
NM_017780.3:c.3779-50G=	NP_060250.2:n.3779-50G=
XM_011517553.1:c.3779-50G=	XP_011515855.1:n.3779-50G=
XM_011517554.1:c.3779-50G=	XP_011515856.1:n.3779-50G=
XM_011517555.1:c.3779-50G=	XP_011515857.1:n.3779-50G=
XM_011517556.1:c.3779-50G=	XP_011515858.1:n.3779-50G=
XM_011517557.1:c.1766-50G=	XP_011515859.1:n.1766-50G=
XM_011517558.1:c.1316-50G=	XP_011515860.1:n.1316-50G=
XM_011517559.1:c.524-50G=	XP_011515861.1:n.524-50G=
XM_011517560.1:c.3779-50G=	XP_011515862.1:n.3779-50G=
XM_011517553.2:c.3779-50G=	XP_011515855.1:n.3779-50G=
XM_011517554.3:c.3779-50G=	XP_011515856.1:n.3779-50G=
XM_011517555.2:c.3779-50G=	XP_011515857.1:n.3779-50G=
XM_011517560.2:c.3779-50G=	XP_011515862.1:n.3779-50G=
XM_017013612.1:c.3779-50G=	XP_016869101.1:n.3779-50G=
XM_017013613.1:c.3779-50G=	XP_016869102.1:n.3779-50G=
NM_017780.4:c.3779-50G= MANE Select	NP_060250.2:n.3779-50G=