Canonical Allele Identifier: CA371323846

Gene: CHD7

Linked Data

• ClinVar Variation Id: 934343
• ClinVar RCV Id: RCV001202710
• dbSNP Id: rs1805502860
• MyVariant Identifiers: chr8:g.61765141C>G (hg19) ; chr8:g.60852582C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60852582C>G , CM000670.2:g.60852582C>G	GRCh38
NC_000008.10:g.61765141C>G , CM000670.1:g.61765141C>G	GRCh37
NC_000008.9:g.61927695C>G	NCBI36
NG_007009.1:g.178803C>G , LRG_176:g.178803C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.5979C>G	ENSP00000512218.1:p.Asp1993Glu
ENST00000423902.7:c.5979C>G MANE Select	ENSP00000392028.1:p.Asp1993Glu
ENST00000423902.6:c.5979C>G	ENSP00000392028.1:p.Asp1993Glu
ENST00000524602.5:c.1717-9647C>G	ENSP00000437061.1:n.1717-9647C>G
ENST00000527921.1:n.470C>G
NM_001316690.1:c.1717-9647C>G	NP_001303619.1:n.1717-9647C>G
NM_017780.3:c.5979C>G	NP_060250.2:p.Asp1993Glu
XM_011517553.1:c.6069C>G	XP_011515855.1:p.Asp2023Glu
XM_011517554.1:c.6069C>G	XP_011515856.1:p.Asp2023Glu
XM_011517555.1:c.6069C>G	XP_011515857.1:p.Asp2023Glu
XM_011517556.1:c.6069C>G	XP_011515858.1:p.Asp2023Glu
XM_011517557.1:c.4056C>G	XP_011515859.1:p.Asp1352Glu
XM_011517558.1:c.3606C>G	XP_011515860.1:p.Asp1202Glu
XM_011517559.1:c.2814C>G	XP_011515861.1:p.Asp938Glu
XM_011517553.2:c.6069C>G	XP_011515855.1:p.Asp2023Glu
XM_011517554.3:c.6069C>G	XP_011515856.1:p.Asp2023Glu
XM_011517555.2:c.6069C>G	XP_011515857.1:p.Asp2023Glu
XM_017013612.1:c.6069C>G	XP_016869101.1:p.Asp2023Glu
XM_017013613.1:c.5979C>G	XP_016869102.1:p.Asp1993Glu
NM_017780.4:c.5979C>G MANE Select	NP_060250.2:p.Asp1993Glu