Canonical Allele Identifier: CA2687400601

Gene: CHD7

Linked Data

• gnomAD v4: 8-60861231-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861231G>T , CM000670.2:g.60861231G>T	GRCh38
NC_000008.10:g.61773790G>T , CM000670.1:g.61773790G>T	GRCh37
NC_000008.9:g.61936344G>T	NCBI36
NG_007009.1:g.187452G>T , LRG_176:g.187452G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.1006+106G>T
ENST00000695851.1:n.210+106G>T
ENST00000695853.1:c.*889+106G>T	ENSP00000512218.1:n.*889+106G>T
ENST00000423902.7:c.7830+106G>T MANE Select	ENSP00000392028.1:n.7830+106G>T
ENST00000423902.6:c.7830+106G>T	ENSP00000392028.1:n.7830+106G>T
ENST00000524602.5:c.1717-998G>T	ENSP00000437061.1:n.1717-998G>T
ENST00000531695.1:n.360G>T
ENST00000618450.1:n.328G>T
NM_001316690.1:c.1717-998G>T	NP_001303619.1:n.1717-998G>T
NM_017780.3:c.7830+106G>T	NP_060250.2:n.7830+106G>T
XM_011517553.1:c.7920+106G>T	XP_011515855.1:n.7920+106G>T
XM_011517554.1:c.7920+106G>T	XP_011515856.1:n.7920+106G>T
XM_011517555.1:c.7917+106G>T	XP_011515857.1:n.7917+106G>T
XM_011517556.1:c.7699-965G>T	XP_011515858.1:n.7699-965G>T
XM_011517557.1:c.5907+106G>T	XP_011515859.1:n.5907+106G>T
XM_011517558.1:c.5457+106G>T	XP_011515860.1:n.5457+106G>T
XM_011517559.1:c.4665+106G>T	XP_011515861.1:n.4665+106G>T
XM_011517553.2:c.7920+106G>T	XP_011515855.1:n.7920+106G>T
XM_011517554.3:c.7920+106G>T	XP_011515856.1:n.7920+106G>T
XM_011517555.2:c.7917+106G>T	XP_011515857.1:n.7917+106G>T
XM_017013612.1:c.7920+106G>T	XP_016869101.1:n.7920+106G>T
XM_017013613.1:c.7827+106G>T	XP_016869102.1:n.7827+106G>T
NM_017780.4:c.7830+106G>T MANE Select	NP_060250.2:n.7830+106G>T