Canonical Allele Identifier: CA1788113986
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60836919G= , CM000670.2:g.60836919G= GRCh38
NC_000008.10:g.61749478G= , CM000670.1:g.61749478G= GRCh37
NC_000008.9:g.61912032G= NCBI36
NG_007009.1:g.163140G= , LRG_176:g.163140G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695853.1:c.4092G= ENSP00000512218.1:p.Leu1364=
ENST00000423902.7:c.4092G= MANE Select ENSP00000392028.1:p.Leu1364=
ENST00000423902.6:c.4092G= ENSP00000392028.1:p.Leu1364=
ENST00000524602.5:c.1717-25310G= ENSP00000437061.1:n.1717-25310G=
NM_001316690.1:c.1717-25310G= NP_001303619.1:n.1717-25310G=
NM_017780.3:c.4092G= NP_060250.2:p.Leu1364=
XM_011517553.1:c.4092G= XP_011515855.1:p.Leu1364=
XM_011517554.1:c.4092G= XP_011515856.1:p.Leu1364=
XM_011517555.1:c.4092G= XP_011515857.1:p.Leu1364=
XM_011517556.1:c.4092G= XP_011515858.1:p.Leu1364=
XM_011517557.1:c.2079G= XP_011515859.1:p.Leu693=
XM_011517558.1:c.1629G= XP_011515860.1:p.Leu543=
XM_011517559.1:c.837G= XP_011515861.1:p.Leu279=
XM_011517560.1:c.4092G= XP_011515862.1:p.Leu1364=
XM_011517553.2:c.4092G= XP_011515855.1:p.Leu1364=
XM_011517554.3:c.4092G= XP_011515856.1:p.Leu1364=
XM_011517555.2:c.4092G= XP_011515857.1:p.Leu1364=
XM_011517560.2:c.4092G= XP_011515862.1:p.Leu1364=
XM_017013612.1:c.4092G= XP_016869101.1:p.Leu1364=
XM_017013613.1:c.4092G= XP_016869102.1:p.Leu1364=
NM_017780.4:c.4092G= MANE Select NP_060250.2:p.Leu1364=