Canonical Allele Identifier: CA371318468

Gene: CHD7

Linked Data

• gnomAD v4: 8-60841645-C-A
• MyVariant Identifiers: chr8:g.61754204C>A (hg19) ; chr8:g.60841645C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60841645C>A , CM000670.2:g.60841645C>A	GRCh38
NC_000008.10:g.61754204C>A , CM000670.1:g.61754204C>A	GRCh37
NC_000008.9:g.61916758C>A	NCBI36
NG_007009.1:g.167866C>A , LRG_176:g.167866C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695853.1:c.4535C>A	ENSP00000512218.1:p.Ala1512Asp
ENST00000423902.7:c.4535C>A MANE Select	ENSP00000392028.1:p.Ala1512Asp
ENST00000423902.6:c.4535C>A	ENSP00000392028.1:p.Ala1512Asp
ENST00000524602.5:c.1717-20584C>A	ENSP00000437061.1:n.1717-20584C>A
NM_001316690.1:c.1717-20584C>A	NP_001303619.1:n.1717-20584C>A
NM_017780.3:c.4535C>A	NP_060250.2:p.Ala1512Asp
XM_011517553.1:c.4535C>A	XP_011515855.1:p.Ala1512Asp
XM_011517554.1:c.4535C>A	XP_011515856.1:p.Ala1512Asp
XM_011517555.1:c.4535C>A	XP_011515857.1:p.Ala1512Asp
XM_011517556.1:c.4535C>A	XP_011515858.1:p.Ala1512Asp
XM_011517557.1:c.2522C>A	XP_011515859.1:p.Ala841Asp
XM_011517558.1:c.2072C>A	XP_011515860.1:p.Ala691Asp
XM_011517559.1:c.1280C>A	XP_011515861.1:p.Ala427Asp
XM_011517560.1:c.4535C>A	XP_011515862.1:p.Ala1512Asp
XM_011517553.2:c.4535C>A	XP_011515855.1:p.Ala1512Asp
XM_011517554.3:c.4535C>A	XP_011515856.1:p.Ala1512Asp
XM_011517555.2:c.4535C>A	XP_011515857.1:p.Ala1512Asp
XM_011517560.2:c.4535C>A	XP_011515862.1:p.Ala1512Asp
XM_017013612.1:c.4535C>A	XP_016869101.1:p.Ala1512Asp
XM_017013613.1:c.4535C>A	XP_016869102.1:p.Ala1512Asp
NM_017780.4:c.4535C>A MANE Select	NP_060250.2:p.Ala1512Asp