Canonical Allele Identifier: CA1788130248
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60865393C= , CM000670.2:g.60865393C= GRCh38
NC_000008.10:g.61777952C= , CM000670.1:g.61777952C= GRCh37
NC_000008.9:g.61940506C= NCBI36
NG_007009.1:g.191614C= , LRG_176:g.191614C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695850.1:n.1630C=
ENST00000695852.1:n.561C=
ENST00000695853.1:c.*1513C= ENSP00000512218.1:n.*1513C=
ENST00000423902.7:c.8454C= MANE Select ENSP00000392028.1:p.Asn2818=
ENST00000423902.6:c.8454C= ENSP00000392028.1:p.Asn2818=
ENST00000524602.5:c.2307C= ENSP00000437061.1:p.Asn769=
ENST00000528280.1:n.500C=
NM_001316690.1:c.2307C= NP_001303619.1:p.Asn769=
NM_017780.3:c.8454C= NP_060250.2:p.Asn2818=
XM_011517553.1:c.8544C= XP_011515855.1:p.Asn2848=
XM_011517554.1:c.8544C= XP_011515856.1:p.Asn2848=
XM_011517555.1:c.8541C= XP_011515857.1:p.Asn2847=
XM_011517556.1:c.8322C= XP_011515858.1:p.Asn2774=
XM_011517557.1:c.6531C= XP_011515859.1:p.Asn2177=
XM_011517558.1:c.6081C= XP_011515860.1:p.Asn2027=
XM_011517559.1:c.5289C= XP_011515861.1:p.Asn1763=
XM_011517553.2:c.8544C= XP_011515855.1:p.Asn2848=
XM_011517554.3:c.8544C= XP_011515856.1:p.Asn2848=
XM_011517555.2:c.8541C= XP_011515857.1:p.Asn2847=
XM_017013612.1:c.8544C= XP_016869101.1:p.Asn2848=
XM_017013613.1:c.8451C= XP_016869102.1:p.Asn2817=
NM_017780.4:c.8454C= MANE Select NP_060250.2:p.Asn2818=