Canonical Allele Identifier: CA1788120767

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860995C= , CM000670.2:g.60860995C=	GRCh38
NC_000008.10:g.61773554C= , CM000670.1:g.61773554C=	GRCh37
NC_000008.9:g.61936108C=	NCBI36
NG_007009.1:g.187216C= , LRG_176:g.187216C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.876C=
ENST00000695851.1:n.80C=
ENST00000695853.1:c.*759C=	ENSP00000512218.1:n.*759C=
ENST00000423902.7:c.7700C= MANE Select	ENSP00000392028.1:p.Thr2567=
ENST00000423902.6:c.7700C=	ENSP00000392028.1:p.Thr2567=
ENST00000524602.5:c.1717-1234C=	ENSP00000437061.1:n.1717-1234C=
ENST00000531695.1:n.124C=
ENST00000618450.1:n.92C=
NM_001316690.1:c.1717-1234C=	NP_001303619.1:n.1717-1234C=
NM_017780.3:c.7700C=	NP_060250.2:p.Thr2567=
XM_011517553.1:c.7790C=	XP_011515855.1:p.Thr2597=
XM_011517554.1:c.7790C=	XP_011515856.1:p.Thr2597=
XM_011517555.1:c.7787C=	XP_011515857.1:p.Thr2596=
XM_011517556.1:c.7699-1201C=	XP_011515858.1:n.7699-1201C=
XM_011517557.1:c.5777C=	XP_011515859.1:p.Thr1926=
XM_011517558.1:c.5327C=	XP_011515860.1:p.Thr1776=
XM_011517559.1:c.4535C=	XP_011515861.1:p.Thr1512=
XM_011517553.2:c.7790C=	XP_011515855.1:p.Thr2597=
XM_011517554.3:c.7790C=	XP_011515856.1:p.Thr2597=
XM_011517555.2:c.7787C=	XP_011515857.1:p.Thr2596=
XM_017013612.1:c.7790C=	XP_016869101.1:p.Thr2597=
XM_017013613.1:c.7697C=	XP_016869102.1:p.Thr2566=
NM_017780.4:c.7700C= MANE Select	NP_060250.2:p.Thr2567=