Canonical Allele Identifier: CA371304209
Gene: CHD7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60860928T>C , CM000670.2:g.60860928T>C GRCh38
NC_000008.10:g.61773487T>C , CM000670.1:g.61773487T>C GRCh37
NC_000008.9:g.61936041T>C NCBI36
NG_007009.1:g.187149T>C , LRG_176:g.187149T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695850.1:n.809T>C
ENST00000695851.1:n.13T>C
ENST00000695853.1:c.*692T>C ENSP00000512218.1:n.*692T>C
ENST00000423902.7:c.7633T>C MANE Select ENSP00000392028.1:p.Phe2545Leu
ENST00000423902.6:c.7633T>C ENSP00000392028.1:p.Phe2545Leu
ENST00000524602.5:c.1717-1301T>C ENSP00000437061.1:n.1717-1301T>C
ENST00000531695.1:n.57T>C
ENST00000618450.1:n.25T>C
NM_001316690.1:c.1717-1301T>C NP_001303619.1:n.1717-1301T>C
NM_017780.3:c.7633T>C NP_060250.2:p.Phe2545Leu
XM_011517553.1:c.7723T>C XP_011515855.1:p.Phe2575Leu
XM_011517554.1:c.7723T>C XP_011515856.1:p.Phe2575Leu
XM_011517555.1:c.7720T>C XP_011515857.1:p.Phe2574Leu
XM_011517556.1:c.7699-1268T>C XP_011515858.1:n.7699-1268T>C
XM_011517557.1:c.5710T>C XP_011515859.1:p.Phe1904Leu
XM_011517558.1:c.5260T>C XP_011515860.1:p.Phe1754Leu
XM_011517559.1:c.4468T>C XP_011515861.1:p.Phe1490Leu
XM_011517553.2:c.7723T>C XP_011515855.1:p.Phe2575Leu
XM_011517554.3:c.7723T>C XP_011515856.1:p.Phe2575Leu
XM_011517555.2:c.7720T>C XP_011515857.1:p.Phe2574Leu
XM_017013612.1:c.7723T>C XP_016869101.1:p.Phe2575Leu
XM_017013613.1:c.7630T>C XP_016869102.1:p.Phe2544Leu
NM_017780.4:c.7633T>C MANE Select NP_060250.2:p.Phe2545Leu