Canonical Allele Identifier: CA1788134880

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60849149A= , CM000670.2:g.60849149A=	GRCh38
NC_000008.10:g.61761708A= , CM000670.1:g.61761708A=	GRCh37
NC_000008.9:g.61924262A=	NCBI36
NG_007009.1:g.175370A= , LRG_176:g.175370A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.5399A=	ENSP00000512218.1:p.Lys1800=
ENST00000423902.7:c.5399A= MANE Select	ENSP00000392028.1:p.Lys1800=
ENST00000423902.6:c.5399A=	ENSP00000392028.1:p.Lys1800=
ENST00000524602.5:c.1717-13080A=	ENSP00000437061.1:n.1717-13080A=
NM_001316690.1:c.1717-13080A=	NP_001303619.1:n.1717-13080A=
NM_017780.3:c.5399A=	NP_060250.2:p.Lys1800=
XM_011517553.1:c.5489A=	XP_011515855.1:p.Lys1830=
XM_011517554.1:c.5489A=	XP_011515856.1:p.Lys1830=
XM_011517555.1:c.5489A=	XP_011515857.1:p.Lys1830=
XM_011517556.1:c.5489A=	XP_011515858.1:p.Lys1830=
XM_011517557.1:c.3476A=	XP_011515859.1:p.Lys1159=
XM_011517558.1:c.3026A=	XP_011515860.1:p.Lys1009=
XM_011517559.1:c.2234A=	XP_011515861.1:p.Lys745=
XM_011517553.2:c.5489A=	XP_011515855.1:p.Lys1830=
XM_011517554.3:c.5489A=	XP_011515856.1:p.Lys1830=
XM_011517555.2:c.5489A=	XP_011515857.1:p.Lys1830=
XM_017013612.1:c.5489A=	XP_016869101.1:p.Lys1830=
XM_017013613.1:c.5399A=	XP_016869102.1:p.Lys1800=
NM_017780.4:c.5399A= MANE Select	NP_060250.2:p.Lys1800=