Canonical Allele Identifier: CA1788130218
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60865390T= , CM000670.2:g.60865390T= GRCh38
NC_000008.10:g.61777949T= , CM000670.1:g.61777949T= GRCh37
NC_000008.9:g.61940503T= NCBI36
NG_007009.1:g.191611T= , LRG_176:g.191611T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695850.1:n.1627T=
ENST00000695852.1:n.558T=
ENST00000695853.1:c.*1510T= ENSP00000512218.1:n.*1510T=
ENST00000423902.7:c.8451T= MANE Select ENSP00000392028.1:p.Asn2817=
ENST00000423902.6:c.8451T= ENSP00000392028.1:p.Asn2817=
ENST00000524602.5:c.2304T= ENSP00000437061.1:p.Asn768=
ENST00000528280.1:n.497T=
NM_001316690.1:c.2304T= NP_001303619.1:p.Asn768=
NM_017780.3:c.8451T= NP_060250.2:p.Asn2817=
XM_011517553.1:c.8541T= XP_011515855.1:p.Asn2847=
XM_011517554.1:c.8541T= XP_011515856.1:p.Asn2847=
XM_011517555.1:c.8538T= XP_011515857.1:p.Asn2846=
XM_011517556.1:c.8319T= XP_011515858.1:p.Asn2773=
XM_011517557.1:c.6528T= XP_011515859.1:p.Asn2176=
XM_011517558.1:c.6078T= XP_011515860.1:p.Asn2026=
XM_011517559.1:c.5286T= XP_011515861.1:p.Asn1762=
XM_011517553.2:c.8541T= XP_011515855.1:p.Asn2847=
XM_011517554.3:c.8541T= XP_011515856.1:p.Asn2847=
XM_011517555.2:c.8538T= XP_011515857.1:p.Asn2846=
XM_017013612.1:c.8541T= XP_016869101.1:p.Asn2847=
XM_017013613.1:c.8448T= XP_016869102.1:p.Asn2816=
NM_017780.4:c.8451T= MANE Select NP_060250.2:p.Asn2817=