Canonical Allele Identifier: CA371304397

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773529T>A (hg19) ; chr8:g.60860970T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60860970T>A , CM000670.2:g.60860970T>A	GRCh38
NC_000008.10:g.61773529T>A , CM000670.1:g.61773529T>A	GRCh37
NC_000008.9:g.61936083T>A	NCBI36
NG_007009.1:g.187191T>A , LRG_176:g.187191T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.851T>A
ENST00000695851.1:n.55T>A
ENST00000695853.1:c.*734T>A	ENSP00000512218.1:n.*734T>A
ENST00000423902.7:c.7675T>A MANE Select	ENSP00000392028.1:p.Ser2559Thr
ENST00000423902.6:c.7675T>A	ENSP00000392028.1:p.Ser2559Thr
ENST00000524602.5:c.1717-1259T>A	ENSP00000437061.1:n.1717-1259T>A
ENST00000531695.1:n.99T>A
ENST00000618450.1:n.67T>A
NM_001316690.1:c.1717-1259T>A	NP_001303619.1:n.1717-1259T>A
NM_017780.3:c.7675T>A	NP_060250.2:p.Ser2559Thr
XM_011517553.1:c.7765T>A	XP_011515855.1:p.Ser2589Thr
XM_011517554.1:c.7765T>A	XP_011515856.1:p.Ser2589Thr
XM_011517555.1:c.7762T>A	XP_011515857.1:p.Ser2588Thr
XM_011517556.1:c.7699-1226T>A	XP_011515858.1:n.7699-1226T>A
XM_011517557.1:c.5752T>A	XP_011515859.1:p.Ser1918Thr
XM_011517558.1:c.5302T>A	XP_011515860.1:p.Ser1768Thr
XM_011517559.1:c.4510T>A	XP_011515861.1:p.Ser1504Thr
XM_011517553.2:c.7765T>A	XP_011515855.1:p.Ser2589Thr
XM_011517554.3:c.7765T>A	XP_011515856.1:p.Ser2589Thr
XM_011517555.2:c.7762T>A	XP_011515857.1:p.Ser2588Thr
XM_017013612.1:c.7765T>A	XP_016869101.1:p.Ser2589Thr
XM_017013613.1:c.7672T>A	XP_016869102.1:p.Ser2558Thr
NM_017780.4:c.7675T>A MANE Select	NP_060250.2:p.Ser2559Thr