Canonical Allele Identifier: CA1788120788

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861003C= , CM000670.2:g.60861003C=	GRCh38
NC_000008.10:g.61773562C= , CM000670.1:g.61773562C=	GRCh37
NC_000008.9:g.61936116C=	NCBI36
NG_007009.1:g.187224C= , LRG_176:g.187224C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.884C=
ENST00000695851.1:n.88C=
ENST00000695853.1:c.*767C=	ENSP00000512218.1:n.*767C=
ENST00000423902.7:c.7708C= MANE Select	ENSP00000392028.1:p.Pro2570=
ENST00000423902.6:c.7708C=	ENSP00000392028.1:p.Pro2570=
ENST00000524602.5:c.1717-1226C=	ENSP00000437061.1:n.1717-1226C=
ENST00000531695.1:n.132C=
ENST00000618450.1:n.100C=
NM_001316690.1:c.1717-1226C=	NP_001303619.1:n.1717-1226C=
NM_017780.3:c.7708C=	NP_060250.2:p.Pro2570=
XM_011517553.1:c.7798C=	XP_011515855.1:p.Pro2600=
XM_011517554.1:c.7798C=	XP_011515856.1:p.Pro2600=
XM_011517555.1:c.7795C=	XP_011515857.1:p.Pro2599=
XM_011517556.1:c.7699-1193C=	XP_011515858.1:n.7699-1193C=
XM_011517557.1:c.5785C=	XP_011515859.1:p.Pro1929=
XM_011517558.1:c.5335C=	XP_011515860.1:p.Pro1779=
XM_011517559.1:c.4543C=	XP_011515861.1:p.Pro1515=
XM_011517553.2:c.7798C=	XP_011515855.1:p.Pro2600=
XM_011517554.3:c.7798C=	XP_011515856.1:p.Pro2600=
XM_011517555.2:c.7795C=	XP_011515857.1:p.Pro2599=
XM_017013612.1:c.7798C=	XP_016869101.1:p.Pro2600=
XM_017013613.1:c.7705C=	XP_016869102.1:p.Pro2569=
NM_017780.4:c.7708C= MANE Select	NP_060250.2:p.Pro2570=