Canonical Allele Identifier: CA371304660

Gene: CHD7

Linked Data

• MyVariant Identifiers: chr8:g.61773624T>A (hg19) ; chr8:g.60861065T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861065T>A , CM000670.2:g.60861065T>A	GRCh38
NC_000008.10:g.61773624T>A , CM000670.1:g.61773624T>A	GRCh37
NC_000008.9:g.61936178T>A	NCBI36
NG_007009.1:g.187286T>A , LRG_176:g.187286T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.946T>A
ENST00000695851.1:n.150T>A
ENST00000695853.1:c.*829T>A	ENSP00000512218.1:n.*829T>A
ENST00000423902.7:c.7770T>A MANE Select	ENSP00000392028.1:p.Asp2590Glu
ENST00000423902.6:c.7770T>A	ENSP00000392028.1:p.Asp2590Glu
ENST00000524602.5:c.1717-1164T>A	ENSP00000437061.1:n.1717-1164T>A
ENST00000531695.1:n.194T>A
ENST00000618450.1:n.162T>A
NM_001316690.1:c.1717-1164T>A	NP_001303619.1:n.1717-1164T>A
NM_017780.3:c.7770T>A	NP_060250.2:p.Asp2590Glu
XM_011517553.1:c.7860T>A	XP_011515855.1:p.Asp2620Glu
XM_011517554.1:c.7860T>A	XP_011515856.1:p.Asp2620Glu
XM_011517555.1:c.7857T>A	XP_011515857.1:p.Asp2619Glu
XM_011517556.1:c.7699-1131T>A	XP_011515858.1:n.7699-1131T>A
XM_011517557.1:c.5847T>A	XP_011515859.1:p.Asp1949Glu
XM_011517558.1:c.5397T>A	XP_011515860.1:p.Asp1799Glu
XM_011517559.1:c.4605T>A	XP_011515861.1:p.Asp1535Glu
XM_011517553.2:c.7860T>A	XP_011515855.1:p.Asp2620Glu
XM_011517554.3:c.7860T>A	XP_011515856.1:p.Asp2620Glu
XM_011517555.2:c.7857T>A	XP_011515857.1:p.Asp2619Glu
XM_017013612.1:c.7860T>A	XP_016869101.1:p.Asp2620Glu
XM_017013613.1:c.7767T>A	XP_016869102.1:p.Asp2589Glu
NM_017780.4:c.7770T>A MANE Select	NP_060250.2:p.Asp2590Glu