Canonical Allele Identifier: CA371304559

Gene: CHD7

Linked Data

• dbSNP Id: rs1805945184
• gnomAD v3: 8-60861021-G-A
• gnomAD v4: 8-60861021-G-A
• MyVariant Identifiers: chr8:g.61773580G>A (hg19) ; chr8:g.60861021G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60861021G>A , CM000670.2:g.60861021G>A	GRCh38
NC_000008.10:g.61773580G>A , CM000670.1:g.61773580G>A	GRCh37
NC_000008.9:g.61936134G>A	NCBI36
NG_007009.1:g.187242G>A , LRG_176:g.187242G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.902G>A
ENST00000695851.1:n.106G>A
ENST00000695853.1:c.*785G>A	ENSP00000512218.1:n.*785G>A
ENST00000423902.7:c.7726G>A MANE Select	ENSP00000392028.1:p.Asp2576Asn
ENST00000423902.6:c.7726G>A	ENSP00000392028.1:p.Asp2576Asn
ENST00000524602.5:c.1717-1208G>A	ENSP00000437061.1:n.1717-1208G>A
ENST00000531695.1:n.150G>A
ENST00000618450.1:n.118G>A
NM_001316690.1:c.1717-1208G>A	NP_001303619.1:n.1717-1208G>A
NM_017780.3:c.7726G>A	NP_060250.2:p.Asp2576Asn
XM_011517553.1:c.7816G>A	XP_011515855.1:p.Asp2606Asn
XM_011517554.1:c.7816G>A	XP_011515856.1:p.Asp2606Asn
XM_011517555.1:c.7813G>A	XP_011515857.1:p.Asp2605Asn
XM_011517556.1:c.7699-1175G>A	XP_011515858.1:n.7699-1175G>A
XM_011517557.1:c.5803G>A	XP_011515859.1:p.Asp1935Asn
XM_011517558.1:c.5353G>A	XP_011515860.1:p.Asp1785Asn
XM_011517559.1:c.4561G>A	XP_011515861.1:p.Asp1521Asn
XM_011517553.2:c.7816G>A	XP_011515855.1:p.Asp2606Asn
XM_011517554.3:c.7816G>A	XP_011515856.1:p.Asp2606Asn
XM_011517555.2:c.7813G>A	XP_011515857.1:p.Asp2605Asn
XM_017013612.1:c.7816G>A	XP_016869101.1:p.Asp2606Asn
XM_017013613.1:c.7723G>A	XP_016869102.1:p.Asp2575Asn
NM_017780.4:c.7726G>A MANE Select	NP_060250.2:p.Asp2576Asn