Canonical Allele Identifier: CA371304459

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773544G>A (hg19) ; chr8:g.60860985G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860985G>A , CM000670.2:g.60860985G>A	GRCh38
NC_000008.10:g.61773544G>A , CM000670.1:g.61773544G>A	GRCh37
NC_000008.9:g.61936098G>A	NCBI36
NG_007009.1:g.187206G>A , LRG_176:g.187206G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.866G>A
ENST00000695851.1:n.70G>A
ENST00000695853.1:c.*749G>A	ENSP00000512218.1:n.*749G>A
ENST00000423902.7:c.7690G>A MANE Select	ENSP00000392028.1:p.Asp2564Asn
ENST00000423902.6:c.7690G>A	ENSP00000392028.1:p.Asp2564Asn
ENST00000524602.5:c.1717-1244G>A	ENSP00000437061.1:n.1717-1244G>A
ENST00000531695.1:n.114G>A
ENST00000618450.1:n.82G>A
NM_001316690.1:c.1717-1244G>A	NP_001303619.1:n.1717-1244G>A
NM_017780.3:c.7690G>A	NP_060250.2:p.Asp2564Asn
XM_011517553.1:c.7780G>A	XP_011515855.1:p.Asp2594Asn
XM_011517554.1:c.7780G>A	XP_011515856.1:p.Asp2594Asn
XM_011517555.1:c.7777G>A	XP_011515857.1:p.Asp2593Asn
XM_011517556.1:c.7699-1211G>A	XP_011515858.1:n.7699-1211G>A
XM_011517557.1:c.5767G>A	XP_011515859.1:p.Asp1923Asn
XM_011517558.1:c.5317G>A	XP_011515860.1:p.Asp1773Asn
XM_011517559.1:c.4525G>A	XP_011515861.1:p.Asp1509Asn
XM_011517553.2:c.7780G>A	XP_011515855.1:p.Asp2594Asn
XM_011517554.3:c.7780G>A	XP_011515856.1:p.Asp2594Asn
XM_011517555.2:c.7777G>A	XP_011515857.1:p.Asp2593Asn
XM_017013612.1:c.7780G>A	XP_016869101.1:p.Asp2594Asn
XM_017013613.1:c.7687G>A	XP_016869102.1:p.Asp2563Asn
NM_017780.4:c.7690G>A MANE Select	NP_060250.2:p.Asp2564Asn