Canonical Allele Identifier: CA371304124

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773464A>G (hg19) ; chr8:g.60860905A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860905A>G , CM000670.2:g.60860905A>G	GRCh38
NC_000008.10:g.61773464A>G , CM000670.1:g.61773464A>G	GRCh37
NC_000008.9:g.61936018A>G	NCBI36
NG_007009.1:g.187126A>G , LRG_176:g.187126A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.786A>G
ENST00000695853.1:c.*669A>G	ENSP00000512218.1:n.*669A>G
ENST00000423902.7:c.7610A>G MANE Select	ENSP00000392028.1:p.Glu2537Gly
ENST00000423902.6:c.7610A>G	ENSP00000392028.1:p.Glu2537Gly
ENST00000524602.5:c.1717-1324A>G	ENSP00000437061.1:n.1717-1324A>G
ENST00000531695.1:n.34A>G
ENST00000618450.1:n.2A>G
NM_001316690.1:c.1717-1324A>G	NP_001303619.1:n.1717-1324A>G
NM_017780.3:c.7610A>G	NP_060250.2:p.Glu2537Gly
XM_011517553.1:c.7700A>G	XP_011515855.1:p.Glu2567Gly
XM_011517554.1:c.7700A>G	XP_011515856.1:p.Glu2567Gly
XM_011517555.1:c.7697A>G	XP_011515857.1:p.Glu2566Gly
XM_011517556.1:c.7699-1291A>G	XP_011515858.1:n.7699-1291A>G
XM_011517557.1:c.5687A>G	XP_011515859.1:p.Glu1896Gly
XM_011517558.1:c.5237A>G	XP_011515860.1:p.Glu1746Gly
XM_011517559.1:c.4445A>G	XP_011515861.1:p.Glu1482Gly
XM_011517553.2:c.7700A>G	XP_011515855.1:p.Glu2567Gly
XM_011517554.3:c.7700A>G	XP_011515856.1:p.Glu2567Gly
XM_011517555.2:c.7697A>G	XP_011515857.1:p.Glu2566Gly
XM_017013612.1:c.7700A>G	XP_016869101.1:p.Glu2567Gly
XM_017013613.1:c.7607A>G	XP_016869102.1:p.Glu2536Gly
NM_017780.4:c.7610A>G MANE Select	NP_060250.2:p.Glu2537Gly