Canonical Allele Identifier: CA371307554

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61777675C>G (hg19) ; chr8:g.60865116C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1353C>G
ENST00000695852.1:n.284C>G
ENST00000695853.1:c.*1236C>G	ENSP00000512218.1:n.*1236C>G
ENST00000423902.7:c.8177C>G MANE Select	ENSP00000392028.1:p.Ala2726Gly
ENST00000423902.6:c.8177C>G	ENSP00000392028.1:p.Ala2726Gly
ENST00000524602.5:c.2030C>G	ENSP00000437061.1:p.Ala677Gly
ENST00000528280.1:n.223C>G
ENST00000532149.1:n.599C>G
ENST00000618450.1:n.4213C>G
NM_001316690.1:c.2030C>G	NP_001303619.1:p.Ala677Gly
NM_017780.3:c.8177C>G	NP_060250.2:p.Ala2726Gly
XM_011517553.1:c.8267C>G	XP_011515855.1:p.Ala2756Gly
XM_011517554.1:c.8267C>G	XP_011515856.1:p.Ala2756Gly
XM_011517555.1:c.8264C>G	XP_011515857.1:p.Ala2755Gly
XM_011517556.1:c.8045C>G	XP_011515858.1:p.Ala2682Gly
XM_011517557.1:c.6254C>G	XP_011515859.1:p.Ala2085Gly
XM_011517558.1:c.5804C>G	XP_011515860.1:p.Ala1935Gly
XM_011517559.1:c.5012C>G	XP_011515861.1:p.Ala1671Gly
XM_011517553.2:c.8267C>G	XP_011515855.1:p.Ala2756Gly
XM_011517554.3:c.8267C>G	XP_011515856.1:p.Ala2756Gly
XM_011517555.2:c.8264C>G	XP_011515857.1:p.Ala2755Gly
XM_017013612.1:c.8267C>G	XP_016869101.1:p.Ala2756Gly
XM_017013613.1:c.8174C>G	XP_016869102.1:p.Ala2725Gly
NM_017780.4:c.8177C>G MANE Select	NP_060250.2:p.Ala2726Gly