Canonical Allele Identifier: CA1788115851

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60837988_60837992delinsCTCTT , CM000670.2:g.60837988_60837992delinsCTCTT	GRCh38
NC_000008.10:g.61750547_61750551delinsCTCTT , CM000670.1:g.61750547_61750551delinsCTCTT	GRCh37
NC_000008.9:g.61913101_61913105delinsCTCTT	NCBI36
NG_007009.1:g.164209_164213delinsCTCTT , LRG_176:g.164209_164213delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.4354-88_4354-84delinsCTCTT	ENSP00000512218.1:n.4354-88_4354-84delinsCTCTT
ENST00000423902.7:c.4354-88_4354-84delinsCTCTT MANE Select	ENSP00000392028.1:n.4354-88_4354-84delinsCTCTT
ENST00000423902.6:c.4354-88_4354-84delinsCTCTT	ENSP00000392028.1:n.4354-88_4354-84delinsCTCTT
ENST00000524602.5:c.1717-24241_1717-24237delinsCTCTT	ENSP00000437061.1:n.1717-24241_1717-24237delinsCTCTT
NM_001316690.1:c.1717-24241_1717-24237delinsCTCTT	NP_001303619.1:n.1717-24241_1717-24237delinsCTCTT
NM_017780.3:c.4354-88_4354-84delinsCTCTT	NP_060250.2:n.4354-88_4354-84delinsCTCTT
XM_011517553.1:c.4354-88_4354-84delinsCTCTT	XP_011515855.1:n.4354-88_4354-84delinsCTCTT
XM_011517554.1:c.4354-88_4354-84delinsCTCTT	XP_011515856.1:n.4354-88_4354-84delinsCTCTT
XM_011517555.1:c.4354-88_4354-84delinsCTCTT	XP_011515857.1:n.4354-88_4354-84delinsCTCTT
XM_011517556.1:c.4354-88_4354-84delinsCTCTT	XP_011515858.1:n.4354-88_4354-84delinsCTCTT
XM_011517557.1:c.2341-88_2341-84delinsCTCTT	XP_011515859.1:n.2341-88_2341-84delinsCTCTT
XM_011517558.1:c.1891-88_1891-84delinsCTCTT	XP_011515860.1:n.1891-88_1891-84delinsCTCTT
XM_011517559.1:c.1099-88_1099-84delinsCTCTT	XP_011515861.1:n.1099-88_1099-84delinsCTCTT
XM_011517560.1:c.4354-88_4354-84delinsCTCTT	XP_011515862.1:n.4354-88_4354-84delinsCTCTT
XM_011517553.2:c.4354-88_4354-84delinsCTCTT	XP_011515855.1:n.4354-88_4354-84delinsCTCTT
XM_011517554.3:c.4354-88_4354-84delinsCTCTT	XP_011515856.1:n.4354-88_4354-84delinsCTCTT
XM_011517555.2:c.4354-88_4354-84delinsCTCTT	XP_011515857.1:n.4354-88_4354-84delinsCTCTT
XM_011517560.2:c.4354-88_4354-84delinsCTCTT	XP_011515862.1:n.4354-88_4354-84delinsCTCTT
XM_017013612.1:c.4354-88_4354-84delinsCTCTT	XP_016869101.1:n.4354-88_4354-84delinsCTCTT
XM_017013613.1:c.4354-88_4354-84delinsCTCTT	XP_016869102.1:n.4354-88_4354-84delinsCTCTT
NM_017780.4:c.4354-88_4354-84delinsCTCTT MANE Select	NP_060250.2:n.4354-88_4354-84delinsCTCTT