Canonical Allele Identifier: CA1788103318
Gene: CHD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60853016C= , CM000670.2:g.60853016C= GRCh38
NC_000008.10:g.61765575C= , CM000670.1:g.61765575C= GRCh37
NC_000008.9:g.61928129C= NCBI36
NG_007009.1:g.179237C= , LRG_176:g.179237C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695853.1:c.6291C= ENSP00000512218.1:p.Asp2097=
ENST00000423902.7:c.6291C= MANE Select ENSP00000392028.1:p.Asp2097=
ENST00000423902.6:c.6291C= ENSP00000392028.1:p.Asp2097=
ENST00000524602.5:c.1717-9213C= ENSP00000437061.1:n.1717-9213C=
NM_001316690.1:c.1717-9213C= NP_001303619.1:n.1717-9213C=
NM_017780.3:c.6291C= NP_060250.2:p.Asp2097=
XM_011517553.1:c.6381C= XP_011515855.1:p.Asp2127=
XM_011517554.1:c.6381C= XP_011515856.1:p.Asp2127=
XM_011517555.1:c.6381C= XP_011515857.1:p.Asp2127=
XM_011517556.1:c.6381C= XP_011515858.1:p.Asp2127=
XM_011517557.1:c.4368C= XP_011515859.1:p.Asp1456=
XM_011517558.1:c.3918C= XP_011515860.1:p.Asp1306=
XM_011517559.1:c.3126C= XP_011515861.1:p.Asp1042=
XM_011517553.2:c.6381C= XP_011515855.1:p.Asp2127=
XM_011517554.3:c.6381C= XP_011515856.1:p.Asp2127=
XM_011517555.2:c.6381C= XP_011515857.1:p.Asp2127=
XM_017013612.1:c.6381C= XP_016869101.1:p.Asp2127=
XM_017013613.1:c.6291C= XP_016869102.1:p.Asp2097=
NM_017780.4:c.6291C= MANE Select NP_060250.2:p.Asp2097=