Canonical Allele Identifier: CA371304595

Gene: CHD7

Linked Data

• dbSNP Id: rs1586460126
• MyVariant Identifiers: chr8:g.61773596T>G (hg19) ; chr8:g.60861037T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861037T>G , CM000670.2:g.60861037T>G	GRCh38
NC_000008.10:g.61773596T>G , CM000670.1:g.61773596T>G	GRCh37
NC_000008.9:g.61936150T>G	NCBI36
NG_007009.1:g.187258T>G , LRG_176:g.187258T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.918T>G
ENST00000695851.1:n.122T>G
ENST00000695853.1:c.*801T>G	ENSP00000512218.1:n.*801T>G
ENST00000423902.7:c.7742T>G MANE Select	ENSP00000392028.1:p.Val2581Gly
ENST00000423902.6:c.7742T>G	ENSP00000392028.1:p.Val2581Gly
ENST00000524602.5:c.1717-1192T>G	ENSP00000437061.1:n.1717-1192T>G
ENST00000531695.1:n.166T>G
ENST00000618450.1:n.134T>G
NM_001316690.1:c.1717-1192T>G	NP_001303619.1:n.1717-1192T>G
NM_017780.3:c.7742T>G	NP_060250.2:p.Val2581Gly
XM_011517553.1:c.7832T>G	XP_011515855.1:p.Val2611Gly
XM_011517554.1:c.7832T>G	XP_011515856.1:p.Val2611Gly
XM_011517555.1:c.7829T>G	XP_011515857.1:p.Val2610Gly
XM_011517556.1:c.7699-1159T>G	XP_011515858.1:n.7699-1159T>G
XM_011517557.1:c.5819T>G	XP_011515859.1:p.Val1940Gly
XM_011517558.1:c.5369T>G	XP_011515860.1:p.Val1790Gly
XM_011517559.1:c.4577T>G	XP_011515861.1:p.Val1526Gly
XM_011517553.2:c.7832T>G	XP_011515855.1:p.Val2611Gly
XM_011517554.3:c.7832T>G	XP_011515856.1:p.Val2611Gly
XM_011517555.2:c.7829T>G	XP_011515857.1:p.Val2610Gly
XM_017013612.1:c.7832T>G	XP_016869101.1:p.Val2611Gly
XM_017013613.1:c.7739T>G	XP_016869102.1:p.Val2580Gly
NM_017780.4:c.7742T>G MANE Select	NP_060250.2:p.Val2581Gly