Canonical Allele Identifier: CA1788120502

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860930T= , CM000670.2:g.60860930T=	GRCh38
NC_000008.10:g.61773489T= , CM000670.1:g.61773489T=	GRCh37
NC_000008.9:g.61936043T=	NCBI36
NG_007009.1:g.187151T= , LRG_176:g.187151T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000695850.1:n.811T=
ENST00000695851.1:n.15T=
ENST00000695853.1:c.*694T=	ENSP00000512218.1:n.*694T=
ENST00000423902.7:c.7635T= MANE Select	ENSP00000392028.1:p.Phe2545=
ENST00000423902.6:c.7635T=	ENSP00000392028.1:p.Phe2545=
ENST00000524602.5:c.1717-1299T=	ENSP00000437061.1:n.1717-1299T=
ENST00000531695.1:n.59T=
ENST00000618450.1:n.27T=
NM_001316690.1:c.1717-1299T=	NP_001303619.1:n.1717-1299T=
NM_017780.3:c.7635T=	NP_060250.2:p.Phe2545=
XM_011517553.1:c.7725T=	XP_011515855.1:p.Phe2575=
XM_011517554.1:c.7725T=	XP_011515856.1:p.Phe2575=
XM_011517555.1:c.7722T=	XP_011515857.1:p.Phe2574=
XM_011517556.1:c.7699-1266T=	XP_011515858.1:n.7699-1266T=
XM_011517557.1:c.5712T=	XP_011515859.1:p.Phe1904=
XM_011517558.1:c.5262T=	XP_011515860.1:p.Phe1754=
XM_011517559.1:c.4470T=	XP_011515861.1:p.Phe1490=
XM_011517553.2:c.7725T=	XP_011515855.1:p.Phe2575=
XM_011517554.3:c.7725T=	XP_011515856.1:p.Phe2575=
XM_011517555.2:c.7722T=	XP_011515857.1:p.Phe2574=
XM_017013612.1:c.7725T=	XP_016869101.1:p.Phe2575=
XM_017013613.1:c.7632T=	XP_016869102.1:p.Phe2544=
NM_017780.4:c.7635T= MANE Select	NP_060250.2:p.Phe2545=