Canonical Allele Identifier: CA115310
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2030
ClinVar RCV Id: RCV000002108
dbSNP Id: rs4738824
gnomAD v2: 8-61690321-A-G
gnomAD v3: 8-60777762-A-G
gnomAD v4: 8-60777762-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60777762A>G , CM000670.2:g.60777762A>G GRCh38
NC_000008.10:g.61690321A>G , CM000670.1:g.61690321A>G GRCh37
NC_000008.9:g.61852875A>G NCBI36
NG_007009.1:g.103983A>G , LRG_176:g.103983A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695848.1:n.2179-3238A>G
ENST00000695849.1:n.2179-3238A>G
ENST00000695853.1:c.1666-3238A>G ENSP00000512218.1:n.1666-3238A>G
ENST00000700671.1:c.1666-3238A>G ENSP00000515139.1:n.1666-3238A>G
ENST00000423902.7:c.1666-3238A>G MANE Select ENSP00000392028.1:n.1666-3238A>G
ENST00000423902.6:c.1666-3238A>G ENSP00000392028.1:n.1666-3238A>G
ENST00000524602.5:c.1666-3238A>G ENSP00000437061.1:n.1666-3238A>G
ENST00000525508.1:c.1666-3238A>G ENSP00000436027.1:n.1666-3238A>G
ENST00000527825.1:c.310-3238A>G
ENST00000527900.1:c.67-3238A>G ENSP00000433336.1:n.67-3238A>G
NM_001316690.1:c.1666-3238A>G NP_001303619.1:n.1666-3238A>G
NM_017780.3:c.1666-3238A>G NP_060250.2:n.1666-3238A>G
XM_011517553.1:c.1666-3238A>G XP_011515855.1:n.1666-3238A>G
XM_011517554.1:c.1666-3238A>G XP_011515856.1:n.1666-3238A>G
XM_011517555.1:c.1666-3238A>G XP_011515857.1:n.1666-3238A>G
XM_011517556.1:c.1666-3238A>G XP_011515858.1:n.1666-3238A>G
XM_011517560.1:c.1666-3238A>G XP_011515862.1:n.1666-3238A>G
XM_011517553.2:c.1666-3238A>G XP_011515855.1:n.1666-3238A>G
XM_011517554.3:c.1666-3238A>G XP_011515856.1:n.1666-3238A>G
XM_011517555.2:c.1666-3238A>G XP_011515857.1:n.1666-3238A>G
XM_011517560.2:c.1666-3238A>G XP_011515862.1:n.1666-3238A>G
XM_017013612.1:c.1666-3238A>G XP_016869101.1:n.1666-3238A>G
XM_017013613.1:c.1666-3238A>G XP_016869102.1:n.1666-3238A>G
NM_017780.4:c.1666-3238A>G MANE Select NP_060250.2:n.1666-3238A>G