Canonical Allele Identifier: CA371307366
Gene: CHD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60865084C>A , CM000670.2:g.60865084C>A GRCh38
NC_000008.10:g.61777643C>A , CM000670.1:g.61777643C>A GRCh37
NC_000008.9:g.61940197C>A NCBI36
NG_007009.1:g.191305C>A , LRG_176:g.191305C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695850.1:n.1321C>A
ENST00000695852.1:n.252C>A
ENST00000695853.1:c.*1204C>A ENSP00000512218.1:n.*1204C>A
ENST00000423902.7:c.8145C>A MANE Select ENSP00000392028.1:p.Ser2715Arg
ENST00000423902.6:c.8145C>A ENSP00000392028.1:p.Ser2715Arg
ENST00000524602.5:c.1998C>A ENSP00000437061.1:p.Ser666Arg
ENST00000528280.1:n.191C>A
ENST00000532149.1:n.567C>A
ENST00000618450.1:n.4181C>A
NM_001316690.1:c.1998C>A NP_001303619.1:p.Ser666Arg
NM_017780.3:c.8145C>A NP_060250.2:p.Ser2715Arg
XM_011517553.1:c.8235C>A XP_011515855.1:p.Ser2745Arg
XM_011517554.1:c.8235C>A XP_011515856.1:p.Ser2745Arg
XM_011517555.1:c.8232C>A XP_011515857.1:p.Ser2744Arg
XM_011517556.1:c.8013C>A XP_011515858.1:p.Ser2671Arg
XM_011517557.1:c.6222C>A XP_011515859.1:p.Ser2074Arg
XM_011517558.1:c.5772C>A XP_011515860.1:p.Ser1924Arg
XM_011517559.1:c.4980C>A XP_011515861.1:p.Ser1660Arg
XM_011517553.2:c.8235C>A XP_011515855.1:p.Ser2745Arg
XM_011517554.3:c.8235C>A XP_011515856.1:p.Ser2745Arg
XM_011517555.2:c.8232C>A XP_011515857.1:p.Ser2744Arg
XM_017013612.1:c.8235C>A XP_016869101.1:p.Ser2745Arg
XM_017013613.1:c.8142C>A XP_016869102.1:p.Ser2714Arg
NM_017780.4:c.8145C>A MANE Select NP_060250.2:p.Ser2715Arg