Canonical Allele Identifier: CA371324467

Gene: CHD7

Linked Data

• gnomAD v4: 8-60852943-A-G
• MyVariant Identifiers: chr8:g.61765502A>G (hg19) ; chr8:g.60852943A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60852943A>G , CM000670.2:g.60852943A>G	GRCh38
NC_000008.10:g.61765502A>G , CM000670.1:g.61765502A>G	GRCh37
NC_000008.9:g.61928056A>G	NCBI36
NG_007009.1:g.179164A>G , LRG_176:g.179164A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695853.1:c.6218A>G	ENSP00000512218.1:p.Gln2073Arg
ENST00000423902.7:c.6218A>G MANE Select	ENSP00000392028.1:p.Gln2073Arg
ENST00000423902.6:c.6218A>G	ENSP00000392028.1:p.Gln2073Arg
ENST00000524602.5:c.1717-9286A>G	ENSP00000437061.1:n.1717-9286A>G
NM_001316690.1:c.1717-9286A>G	NP_001303619.1:n.1717-9286A>G
NM_017780.3:c.6218A>G	NP_060250.2:p.Gln2073Arg
XM_011517553.1:c.6308A>G	XP_011515855.1:p.Gln2103Arg
XM_011517554.1:c.6308A>G	XP_011515856.1:p.Gln2103Arg
XM_011517555.1:c.6308A>G	XP_011515857.1:p.Gln2103Arg
XM_011517556.1:c.6308A>G	XP_011515858.1:p.Gln2103Arg
XM_011517557.1:c.4295A>G	XP_011515859.1:p.Gln1432Arg
XM_011517558.1:c.3845A>G	XP_011515860.1:p.Gln1282Arg
XM_011517559.1:c.3053A>G	XP_011515861.1:p.Gln1018Arg
XM_011517553.2:c.6308A>G	XP_011515855.1:p.Gln2103Arg
XM_011517554.3:c.6308A>G	XP_011515856.1:p.Gln2103Arg
XM_011517555.2:c.6308A>G	XP_011515857.1:p.Gln2103Arg
XM_017013612.1:c.6308A>G	XP_016869101.1:p.Gln2103Arg
XM_017013613.1:c.6218A>G	XP_016869102.1:p.Gln2073Arg
NM_017780.4:c.6218A>G MANE Select	NP_060250.2:p.Gln2073Arg