Canonical Allele Identifier: CA371321009
Gene: CHD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60849055G>A , CM000670.2:g.60849055G>A GRCh38
NC_000008.10:g.61761614G>A , CM000670.1:g.61761614G>A GRCh37
NC_000008.9:g.61924168G>A NCBI36
NG_007009.1:g.175276G>A , LRG_176:g.175276G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695853.1:c.5305G>A ENSP00000512218.1:p.Ala1769Thr
ENST00000423902.7:c.5305G>A MANE Select ENSP00000392028.1:p.Ala1769Thr
ENST00000423902.6:c.5305G>A ENSP00000392028.1:p.Ala1769Thr
ENST00000524602.5:c.1717-13174G>A ENSP00000437061.1:n.1717-13174G>A
NM_001316690.1:c.1717-13174G>A NP_001303619.1:n.1717-13174G>A
NM_017780.3:c.5305G>A NP_060250.2:p.Ala1769Thr
XM_011517553.1:c.5395G>A XP_011515855.1:p.Ala1799Thr
XM_011517554.1:c.5395G>A XP_011515856.1:p.Ala1799Thr
XM_011517555.1:c.5395G>A XP_011515857.1:p.Ala1799Thr
XM_011517556.1:c.5395G>A XP_011515858.1:p.Ala1799Thr
XM_011517557.1:c.3382G>A XP_011515859.1:p.Ala1128Thr
XM_011517558.1:c.2932G>A XP_011515860.1:p.Ala978Thr
XM_011517559.1:c.2140G>A XP_011515861.1:p.Ala714Thr
XM_011517553.2:c.5395G>A XP_011515855.1:p.Ala1799Thr
XM_011517554.3:c.5395G>A XP_011515856.1:p.Ala1799Thr
XM_011517555.2:c.5395G>A XP_011515857.1:p.Ala1799Thr
XM_017013612.1:c.5395G>A XP_016869101.1:p.Ala1799Thr
XM_017013613.1:c.5305G>A XP_016869102.1:p.Ala1769Thr
NM_017780.4:c.5305G>A MANE Select NP_060250.2:p.Ala1769Thr