Canonical Allele Identifier: CA1788133707

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60848560G= , CM000670.2:g.60848560G=	GRCh38
NC_000008.10:g.61761119G= , CM000670.1:g.61761119G=	GRCh37
NC_000008.9:g.61923673G=	NCBI36
NG_007009.1:g.174781G= , LRG_176:g.174781G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.5256G=	ENSP00000512218.1:p.Val1752=
ENST00000423902.7:c.5256G= MANE Select	ENSP00000392028.1:p.Val1752=
ENST00000423902.6:c.5256G=	ENSP00000392028.1:p.Val1752=
ENST00000524602.5:c.1717-13669G=	ENSP00000437061.1:n.1717-13669G=
NM_001316690.1:c.1717-13669G=	NP_001303619.1:n.1717-13669G=
NM_017780.3:c.5256G=	NP_060250.2:p.Val1752=
XM_011517553.1:c.5346G=	XP_011515855.1:p.Val1782=
XM_011517554.1:c.5346G=	XP_011515856.1:p.Val1782=
XM_011517555.1:c.5346G=	XP_011515857.1:p.Val1782=
XM_011517556.1:c.5346G=	XP_011515858.1:p.Val1782=
XM_011517557.1:c.3333G=	XP_011515859.1:p.Val1111=
XM_011517558.1:c.2883G=	XP_011515860.1:p.Val961=
XM_011517559.1:c.2091G=	XP_011515861.1:p.Val697=
XM_011517553.2:c.5346G=	XP_011515855.1:p.Val1782=
XM_011517554.3:c.5346G=	XP_011515856.1:p.Val1782=
XM_011517555.2:c.5346G=	XP_011515857.1:p.Val1782=
XM_017013612.1:c.5346G=	XP_016869101.1:p.Val1782=
XM_017013613.1:c.5256G=	XP_016869102.1:p.Val1752=
NM_017780.4:c.5256G= MANE Select	NP_060250.2:p.Val1752=