Canonical Allele Identifier: CA460848374

Gene: CHD7

Linked Data

• dbSNP Id: rs1805310805
• gnomAD v4: 8-60848527-T-A
• MyVariant Identifiers: chr8:g.61761086T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60848527T>A , CM000670.2:g.60848527T>A	GRCh38
NC_000008.10:g.61761086T>A , CM000670.1:g.61761086T>A	GRCh37
NC_000008.9:g.61923640T>A	NCBI36
NG_007009.1:g.174748T>A , LRG_176:g.174748T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.5223T>A	ENSP00000512218.1:p.Arg1741=
ENST00000423902.7:c.5223T>A MANE Select	ENSP00000392028.1:p.Arg1741=
ENST00000423902.6:c.5223T>A	ENSP00000392028.1:p.Arg1741=
ENST00000524602.5:c.1717-13702T>A	ENSP00000437061.1:n.1717-13702T>A
NM_001316690.1:c.1717-13702T>A	NP_001303619.1:n.1717-13702T>A
NM_017780.3:c.5223T>A	NP_060250.2:p.Arg1741=
XM_011517553.1:c.5313T>A	XP_011515855.1:p.Arg1771=
XM_011517554.1:c.5313T>A	XP_011515856.1:p.Arg1771=
XM_011517555.1:c.5313T>A	XP_011515857.1:p.Arg1771=
XM_011517556.1:c.5313T>A	XP_011515858.1:p.Arg1771=
XM_011517557.1:c.3300T>A	XP_011515859.1:p.Arg1100=
XM_011517558.1:c.2850T>A	XP_011515860.1:p.Arg950=
XM_011517559.1:c.2058T>A	XP_011515861.1:p.Arg686=
XM_011517553.2:c.5313T>A	XP_011515855.1:p.Arg1771=
XM_011517554.3:c.5313T>A	XP_011515856.1:p.Arg1771=
XM_011517555.2:c.5313T>A	XP_011515857.1:p.Arg1771=
XM_017013612.1:c.5313T>A	XP_016869101.1:p.Arg1771=
XM_017013613.1:c.5223T>A	XP_016869102.1:p.Arg1741=
NM_017780.4:c.5223T>A MANE Select	NP_060250.2:p.Arg1741=