Canonical Allele Identifier: CA371307553

Gene: CHD7

Linked Data

• gnomAD v4: 8-60865116-C-A
• MyVariant Identifiers: chr8:g.61777675C>A (hg19) ; chr8:g.60865116C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60865116C>A , CM000670.2:g.60865116C>A	GRCh38
NC_000008.10:g.61777675C>A , CM000670.1:g.61777675C>A	GRCh37
NC_000008.9:g.61940229C>A	NCBI36
NG_007009.1:g.191337C>A , LRG_176:g.191337C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1353C>A
ENST00000695852.1:n.284C>A
ENST00000695853.1:c.*1236C>A	ENSP00000512218.1:n.*1236C>A
ENST00000423902.7:c.8177C>A MANE Select	ENSP00000392028.1:p.Ala2726Asp
ENST00000423902.6:c.8177C>A	ENSP00000392028.1:p.Ala2726Asp
ENST00000524602.5:c.2030C>A	ENSP00000437061.1:p.Ala677Asp
ENST00000528280.1:n.223C>A
ENST00000532149.1:n.599C>A
ENST00000618450.1:n.4213C>A
NM_001316690.1:c.2030C>A	NP_001303619.1:p.Ala677Asp
NM_017780.3:c.8177C>A	NP_060250.2:p.Ala2726Asp
XM_011517553.1:c.8267C>A	XP_011515855.1:p.Ala2756Asp
XM_011517554.1:c.8267C>A	XP_011515856.1:p.Ala2756Asp
XM_011517555.1:c.8264C>A	XP_011515857.1:p.Ala2755Asp
XM_011517556.1:c.8045C>A	XP_011515858.1:p.Ala2682Asp
XM_011517557.1:c.6254C>A	XP_011515859.1:p.Ala2085Asp
XM_011517558.1:c.5804C>A	XP_011515860.1:p.Ala1935Asp
XM_011517559.1:c.5012C>A	XP_011515861.1:p.Ala1671Asp
XM_011517553.2:c.8267C>A	XP_011515855.1:p.Ala2756Asp
XM_011517554.3:c.8267C>A	XP_011515856.1:p.Ala2756Asp
XM_011517555.2:c.8264C>A	XP_011515857.1:p.Ala2755Asp
XM_017013612.1:c.8267C>A	XP_016869101.1:p.Ala2756Asp
XM_017013613.1:c.8174C>A	XP_016869102.1:p.Ala2725Asp
NM_017780.4:c.8177C>A MANE Select	NP_060250.2:p.Ala2726Asp