Canonical Allele Identifier: CA371304563

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773581A>G (hg19) ; chr8:g.60861022A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861022A>G , CM000670.2:g.60861022A>G	GRCh38
NC_000008.10:g.61773581A>G , CM000670.1:g.61773581A>G	GRCh37
NC_000008.9:g.61936135A>G	NCBI36
NG_007009.1:g.187243A>G , LRG_176:g.187243A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.903A>G
ENST00000695851.1:n.107A>G
ENST00000695853.1:c.*786A>G	ENSP00000512218.1:n.*786A>G
ENST00000423902.7:c.7727A>G MANE Select	ENSP00000392028.1:p.Asp2576Gly
ENST00000423902.6:c.7727A>G	ENSP00000392028.1:p.Asp2576Gly
ENST00000524602.5:c.1717-1207A>G	ENSP00000437061.1:n.1717-1207A>G
ENST00000531695.1:n.151A>G
ENST00000618450.1:n.119A>G
NM_001316690.1:c.1717-1207A>G	NP_001303619.1:n.1717-1207A>G
NM_017780.3:c.7727A>G	NP_060250.2:p.Asp2576Gly
XM_011517553.1:c.7817A>G	XP_011515855.1:p.Asp2606Gly
XM_011517554.1:c.7817A>G	XP_011515856.1:p.Asp2606Gly
XM_011517555.1:c.7814A>G	XP_011515857.1:p.Asp2605Gly
XM_011517556.1:c.7699-1174A>G	XP_011515858.1:n.7699-1174A>G
XM_011517557.1:c.5804A>G	XP_011515859.1:p.Asp1935Gly
XM_011517558.1:c.5354A>G	XP_011515860.1:p.Asp1785Gly
XM_011517559.1:c.4562A>G	XP_011515861.1:p.Asp1521Gly
XM_011517553.2:c.7817A>G	XP_011515855.1:p.Asp2606Gly
XM_011517554.3:c.7817A>G	XP_011515856.1:p.Asp2606Gly
XM_011517555.2:c.7814A>G	XP_011515857.1:p.Asp2605Gly
XM_017013612.1:c.7817A>G	XP_016869101.1:p.Asp2606Gly
XM_017013613.1:c.7724A>G	XP_016869102.1:p.Asp2575Gly
NM_017780.4:c.7727A>G MANE Select	NP_060250.2:p.Asp2576Gly