Canonical Allele Identifier: CA2580078871

Gene: CHD7

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60855956A>G , CM000670.2:g.60855956A>G	GRCh38
NC_000008.10:g.61768515A>G , CM000670.1:g.61768515A>G	GRCh37
NC_000008.9:g.61931069A>G	NCBI36
NG_007009.1:g.182177A>G , LRG_176:g.182177A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695850.1:n.113-19A>G
ENST00000695853.1:c.6776-19A>G	ENSP00000512218.1:n.6776-19A>G
ENST00000423902.7:c.6937-19A>G MANE Select	ENSP00000392028.1:n.6937-19A>G
ENST00000423902.6:c.6937-19A>G	ENSP00000392028.1:n.6937-19A>G
ENST00000524602.5:c.1717-6273A>G	ENSP00000437061.1:n.1717-6273A>G
ENST00000529472.1:n.118-19A>G
NM_001316690.1:c.1717-6273A>G	NP_001303619.1:n.1717-6273A>G
NM_017780.3:c.6937-19A>G	NP_060250.2:n.6937-19A>G
XM_011517553.1:c.7027-19A>G	XP_011515855.1:n.7027-19A>G
XM_011517554.1:c.7027-19A>G	XP_011515856.1:n.7027-19A>G
XM_011517555.1:c.7024-19A>G	XP_011515857.1:n.7024-19A>G
XM_011517556.1:c.7027-19A>G	XP_011515858.1:n.7027-19A>G
XM_011517557.1:c.5014-19A>G	XP_011515859.1:n.5014-19A>G
XM_011517558.1:c.4564-19A>G	XP_011515860.1:n.4564-19A>G
XM_011517559.1:c.3772-19A>G	XP_011515861.1:n.3772-19A>G
XM_011517553.2:c.7027-19A>G	XP_011515855.1:n.7027-19A>G
XM_011517554.3:c.7027-19A>G	XP_011515856.1:n.7027-19A>G
XM_011517555.2:c.7024-19A>G	XP_011515857.1:n.7024-19A>G
XM_017013612.1:c.7027-19A>G	XP_016869101.1:n.7027-19A>G
XM_017013613.1:c.6934-19A>G	XP_016869102.1:n.6934-19A>G
NM_017780.4:c.6937-19A>G MANE Select	NP_060250.2:n.6937-19A>G