Canonical Allele Identifier: CA371304220
Gene: CHD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60860930T>G , CM000670.2:g.60860930T>G GRCh38
NC_000008.10:g.61773489T>G , CM000670.1:g.61773489T>G GRCh37
NC_000008.9:g.61936043T>G NCBI36
NG_007009.1:g.187151T>G , LRG_176:g.187151T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695850.1:n.811T>G
ENST00000695851.1:n.15T>G
ENST00000695853.1:c.*694T>G ENSP00000512218.1:n.*694T>G
ENST00000423902.7:c.7635T>G MANE Select ENSP00000392028.1:p.Phe2545Leu
ENST00000423902.6:c.7635T>G ENSP00000392028.1:p.Phe2545Leu
ENST00000524602.5:c.1717-1299T>G ENSP00000437061.1:n.1717-1299T>G
ENST00000531695.1:n.59T>G
ENST00000618450.1:n.27T>G
NM_001316690.1:c.1717-1299T>G NP_001303619.1:n.1717-1299T>G
NM_017780.3:c.7635T>G NP_060250.2:p.Phe2545Leu
XM_011517553.1:c.7725T>G XP_011515855.1:p.Phe2575Leu
XM_011517554.1:c.7725T>G XP_011515856.1:p.Phe2575Leu
XM_011517555.1:c.7722T>G XP_011515857.1:p.Phe2574Leu
XM_011517556.1:c.7699-1266T>G XP_011515858.1:n.7699-1266T>G
XM_011517557.1:c.5712T>G XP_011515859.1:p.Phe1904Leu
XM_011517558.1:c.5262T>G XP_011515860.1:p.Phe1754Leu
XM_011517559.1:c.4470T>G XP_011515861.1:p.Phe1490Leu
XM_011517553.2:c.7725T>G XP_011515855.1:p.Phe2575Leu
XM_011517554.3:c.7725T>G XP_011515856.1:p.Phe2575Leu
XM_011517555.2:c.7722T>G XP_011515857.1:p.Phe2574Leu
XM_017013612.1:c.7725T>G XP_016869101.1:p.Phe2575Leu
XM_017013613.1:c.7632T>G XP_016869102.1:p.Phe2544Leu
NM_017780.4:c.7635T>G MANE Select NP_060250.2:p.Phe2545Leu