Canonical Allele Identifier: CA460846569

Gene: CHD7

Linked Data

• gnomAD v4: 8-60861089-C-T
• MyVariant Identifiers: chr8:g.61773648C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861089C>T , CM000670.2:g.60861089C>T	GRCh38
NC_000008.10:g.61773648C>T , CM000670.1:g.61773648C>T	GRCh37
NC_000008.9:g.61936202C>T	NCBI36
NG_007009.1:g.187310C>T , LRG_176:g.187310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.970C>T
ENST00000695851.1:n.174C>T
ENST00000695853.1:c.*853C>T	ENSP00000512218.1:n.*853C>T
ENST00000423902.7:c.7794C>T MANE Select	ENSP00000392028.1:p.His2598=
ENST00000423902.6:c.7794C>T	ENSP00000392028.1:p.His2598=
ENST00000524602.5:c.1717-1140C>T	ENSP00000437061.1:n.1717-1140C>T
ENST00000531695.1:n.218C>T
ENST00000618450.1:n.186C>T
NM_001316690.1:c.1717-1140C>T	NP_001303619.1:n.1717-1140C>T
NM_017780.3:c.7794C>T	NP_060250.2:p.His2598=
XM_011517553.1:c.7884C>T	XP_011515855.1:p.His2628=
XM_011517554.1:c.7884C>T	XP_011515856.1:p.His2628=
XM_011517555.1:c.7881C>T	XP_011515857.1:p.His2627=
XM_011517556.1:c.7699-1107C>T	XP_011515858.1:n.7699-1107C>T
XM_011517557.1:c.5871C>T	XP_011515859.1:p.His1957=
XM_011517558.1:c.5421C>T	XP_011515860.1:p.His1807=
XM_011517559.1:c.4629C>T	XP_011515861.1:p.His1543=
XM_011517553.2:c.7884C>T	XP_011515855.1:p.His2628=
XM_011517554.3:c.7884C>T	XP_011515856.1:p.His2628=
XM_011517555.2:c.7881C>T	XP_011515857.1:p.His2627=
XM_017013612.1:c.7884C>T	XP_016869101.1:p.His2628=
XM_017013613.1:c.7791C>T	XP_016869102.1:p.His2597=
NM_017780.4:c.7794C>T MANE Select	NP_060250.2:p.His2598=