Canonical Allele Identifier: CA1788103549

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60853062G= , CM000670.2:g.60853062G=	GRCh38
NC_000008.10:g.61765621G= , CM000670.1:g.61765621G=	GRCh37
NC_000008.9:g.61928175G=	NCBI36
NG_007009.1:g.179283G= , LRG_176:g.179283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.6337G=	ENSP00000512218.1:p.Asp2113=
ENST00000423902.7:c.6337G= MANE Select	ENSP00000392028.1:p.Asp2113=
ENST00000423902.6:c.6337G=	ENSP00000392028.1:p.Asp2113=
ENST00000524602.5:c.1717-9167G=	ENSP00000437061.1:n.1717-9167G=
NM_001316690.1:c.1717-9167G=	NP_001303619.1:n.1717-9167G=
NM_017780.3:c.6337G=	NP_060250.2:p.Asp2113=
XM_011517553.1:c.6427G=	XP_011515855.1:p.Asp2143=
XM_011517554.1:c.6427G=	XP_011515856.1:p.Asp2143=
XM_011517555.1:c.6427G=	XP_011515857.1:p.Asp2143=
XM_011517556.1:c.6427G=	XP_011515858.1:p.Asp2143=
XM_011517557.1:c.4414G=	XP_011515859.1:p.Asp1472=
XM_011517558.1:c.3964G=	XP_011515860.1:p.Asp1322=
XM_011517559.1:c.3172G=	XP_011515861.1:p.Asp1058=
XM_011517553.2:c.6427G=	XP_011515855.1:p.Asp2143=
XM_011517554.3:c.6427G=	XP_011515856.1:p.Asp2143=
XM_011517555.2:c.6427G=	XP_011515857.1:p.Asp2143=
XM_017013612.1:c.6427G=	XP_016869101.1:p.Asp2143=
XM_017013613.1:c.6337G=	XP_016869102.1:p.Asp2113=
NM_017780.4:c.6337G= MANE Select	NP_060250.2:p.Asp2113=